СÖíÊÓƵapp

Table of Contents

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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 10-Q
(Mark One)
Ìý Ìý Ìý
þ Ìý QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended SeptemberÌý30, 2010.
OR
Ìý Ìý Ìý
o Ìý TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ________ to _______.
Commission file number 001-33528
СÖíÊÓƵapp Health, Inc.
(Exact Name of Registrant as Specified in Its Charter)
Ìý Ìý Ìý
Delaware Ìý 75-2402409
Ìý Ìý Ìý
(State or Other Jurisdiction of
Incorporation or Organization)
Ìý (I.R.S. Employer Identification No.)
4400 Biscayne Blvd.
Miami, FL 33137
(Address of Principal Executive Offices) (Zip Code)
(305)Ìý575-4100
(RegistrantÂ’s Telephone Number, Including Area Code)
Indicate by check mark whether the registrant: (1)Ìýhas filed all reports required to be filed by SectionÌý13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12Ìýmonths (or for such shorter period that the registrant was required to file such reports), and (2)Ìýhas been subject to such filing requirements for the past 90Ìýdays. þ YES o NO
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Website, if any, every Interactive Data File required to be submitted and posted pursuant to RuleÌý405 of RegulationÌýS-T during the preceding 12Ìýmonths (or for such shorter period that the registrant was required to submit and post such files).
YES o NO o
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” (in RuleÌý12b-2 of the Exchange Act) (Check one):
Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Large accelerated filer o Ìý Accelerated filer þ Ìý Non-accelerated filer o Ìý Smaller reporting company o
Ìý Ìý Ìý Ìý (Do not check if a smaller reporting company) Ìý Ìý
Indicate by check mark whether the registrant is a shell company (as defined in RuleÌý12b-2 of the Exchange Act):
YES o NO þ
As of NovemberÌý3, 2010, the registrant had 255,356,326 shares of common stock outstanding.
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ÌýEX-31.1
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ÌýEX-32.1
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CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS
ÌýÌýÌýÌýÌýThis Quarterly Report on Form 10-Q contains “forward-looking statements,” as that term is defined under the Private Securities Litigation Reform Act of 1995, or PSLRA, SectionÌý27A of the Securities Act of 1933, as amended, and SectionÌý21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements include statements about our expectations, beliefs or intentions regarding our product development efforts, business, financial condition, results of operations, strategies or prospects. You can identify forward-looking statements by the fact that these statements do not relate strictly to historical or current matters. Rather, forward-looking statements relate to anticipated or expected events, activities, trends or results as of the date they are made. Because forward-looking statements relate to matters that have not yet occurred, these statements are inherently subject to risks and uncertainties that could cause our actual results to differ materially from any future results expressed or implied by the forward-looking statements. Many factors could cause our actual activities or results to differ materially from the activities and results anticipated in forward-looking statements. These factors include those described below and in “ItemÌý1A-Risk Factors” of our Annual Report on Form 10-K for the year ended DecemberÌý31, 2009, and described from time to time in our reports filed with the Securities and Exchange Commission. Except as required by law, we do not undertake any obligation to update forward-looking statements. We intend that all forward-looking statements be subject to the safe-harbor provisions of the PSLRA. These forward-looking statements are only predictions and reflect our views as of the date they are made with respect to future events and financial performance.
ÌýÌýÌýÌýÌýRisks and uncertainties, the occurrence of which could adversely affect our business, include the following:
Ìý Éù Ìý We have a history of operating losses and we do not expect to become profitable in the near future.
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Ìý Éù Ìý Our technologies are in an early stage of development and are unproven.
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Ìý Éù Ìý Our drug research and development activities may not result in commercially viable products.
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Ìý Éù Ìý The results of previous clinical trials may not be predictive of future results, and our current and planned clinical trials may not satisfy the requirements of the FDA or other non-U.S. regulatory authorities.
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Ìý Éù Ìý We will require substantial additional funding, which may not be available to us on acceptable terms, or at all.
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Ìý Éù Ìý We expect to finance future cash needs primarily through public or private offerings, debt financings or strategic collaborations, which may dilute your stockholdings in the Company.
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Ìý Éù Ìý If our competitors develop and market products that are more effective, safer or less expensive than our future product candidates, our commercial opportunities will be negatively impacted.
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Ìý Éù Ìý The regulatory approval process is expensive, time consuming and uncertain and may prevent us or our collaboration partners from obtaining approvals for the commercialization of some or all of our product candidates.
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Ìý Éù Ìý Failure to recruit and enroll patients for clinical trials may cause the development of our product candidates to be delayed.
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Ìý Éù Ìý Even if we obtain regulatory approvals for our product candidates, the terms of approvals and ongoing regulation of our products may limit how we manufacture and market our product candidates, which could materially impair our ability to generate anticipated revenues.
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Ìý Éù Ìý We may not meet regulatory quality standards applicable to our manufacturing and quality processes.
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Ìý Éù Ìý Even if we receive regulatory approval to market our product candidates, the market may not be receptive to our products.
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Ìý Éù Ìý If we fail to attract and retain key management and scientific personnel, we may be unable to successfully develop or commercialize our product candidates.

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Ìý Éù Ìý In the event that we successfully evolve from a company primarily involved in development to a company also involved in commercialization, we may encounter difficulties in managing our growth and expanding our operations successfully.
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Ìý Éù Ìý If we fail to acquire and develop other products or product candidates, at all or on commercially reasonable terms, we may be unable to diversify or grow our business.
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Ìý Éù Ìý We have no experience manufacturing our pharmaceutical product candidates other than at our Mexican facility and we therefore rely on third parties to manufacture and supply our pharmaceutical product candidates, and would need to meet various standards necessary to satisfy FDA regulations if and when we commence manufacturing.
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Ìý Éù Ìý We currently have no pharmaceutical marketing, sales or distribution organization other than in Chile and Mexico. If we are unable to develop our sales and marketing and distribution capability on our own or through collaborations with marketing partners, we will not be successful in commercializing our pharmaceutical product candidates.
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Ìý Éù Ìý Independent clinical investigators and contract research organizations that we engage to conduct our clinical trials may not be diligent, careful or timely.
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Ìý Éù Ìý The success of our business is dependent on the actions of our collaborative partners.
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Ìý Éù Ìý If we are unable to obtain and enforce patent protection for our products, our business could be materially harmed.
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Ìý Éù Ìý If we are unable to protect the confidentiality of our proprietary information and know-how, the value of our technology and products could be adversely affected.
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Ìý Éù Ìý We rely heavily on licenses from third parties.
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Ìý Éù Ìý We license patent rights to certain of our technology from third-party owners. If such owners do not properly maintain or enforce the patents underlying such licenses, our competitive position and business prospects will be harmed.
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Ìý Éù Ìý Our commercial success depends significantly on our ability to operate without infringing the patents and other proprietary rights of third parties.
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Ìý Éù Ìý Adverse results in material litigation matters or governmental inquiries could have a material adverse effect upon our business and financial condition.
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Ìý Éù Ìý Medicare prescription drug coverage legislation and future legislative or regulatory reform of the health care system may affect our ability to sell our products profitably.
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Ìý Éù Ìý Failure to obtain regulatory approval outside the United States will prevent us from marketing our product candidates abroad.
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Ìý Éù Ìý We may not have the funding available to pursue acquisitions.
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Ìý Éù Ìý Acquisitions may disrupt our business, distract our management and may not proceed as planned; and we may encounter difficulties in integrating acquired businesses.
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Ìý Éù Ìý Non-U.S. governments often impose strict price controls, which may adversely affect our future profitability.
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Ìý Éù Ìý Our business may become subject to legal, economic, political, regulatory and other risks associated with international operations.
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Ìý Éù Ìý The market price of our common stock may fluctuate significantly.

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Ìý Éù Ìý Directors, executive officers, principal stockholders and affiliated entities own a significant percentage of our capital stock, and they may make decisions that you do not consider to be in the best interests of our stockholders.
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Ìý Éù Ìý Compliance with changing regulations concerning corporate governance and public disclosure may result in additional expenses.
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Ìý Éù Ìý If we are unable to satisfy the requirements of SectionÌý404 of the Sarbanes-Oxley Act of 2002, as they apply to us, or our internal controls over financial reporting are not effective, the reliability of our financial statements may be questioned and our common stock price may suffer.
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Ìý Éù Ìý We may be unable to maintain our listing on the NYSE Amex, which could cause our stock price to fall and decrease the liquidity of our common stock.
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Ìý Éù Ìý Future issuances of common stock, including as a result of the conversion of shares of our preferred stock or exercise of warrants and hedging activities may depress the trading price of our common stock.
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Ìý Éù Ìý Provisions in our charter documents and Delaware law could discourage an acquisition of us by a third party, even if the acquisition would be favorable to you.
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Ìý Éù Ìý We do not intend to pay cash dividends on our common stock in the foreseeable future.

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PART I. FINANCIAL INFORMATION
ÌýÌýÌýÌýÌýUnless the context otherwise requires, all references in this Quarterly Report on Form 10-Q to the “Company”, “СÖíÊÓƵapp”, “we”, “our”, “ours”, and “us” refer to СÖíÊÓƵapp Health, Inc., a Delaware corporation, including our wholly-owned subsidiaries.
ItemÌý1. Financial Statements
СÖíÊÓƵapp Health, Inc. and Subsidiaries
CONDENSED CONSOLIDATED BALANCE SHEETS
(unaudited)
(in thousands except share data)
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý Ìý Ìý Ìý December 31, 2009 Ìý
Ìý Ìý September 30, 2010 Ìý Ìý (restated, Refer to NoteÌý12) Ìý
ASSETS
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Current assets
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Cash and cash equivalents
Ìý $ 15,177 Ìý Ìý $ 42,658 Ìý
Accounts receivable, net
Ìý Ìý 13,488 Ìý Ìý Ìý 8,767 Ìý
Inventory, net
Ìý Ìý 13,868 Ìý Ìý Ìý 10,520 Ìý
Prepaid expenses and other current assets
Ìý Ìý 2,321 Ìý Ìý Ìý 1,873 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total current assets
Ìý Ìý 44,854 Ìý Ìý Ìý 63,818 Ìý
Property, plant and equipment, net
Ìý Ìý 2,548 Ìý Ìý Ìý 593 Ìý
Intangible assets, net
Ìý Ìý 10,578 Ìý Ìý Ìý 12,722 Ìý
Goodwill
Ìý Ìý 5,652 Ìý Ìý Ìý 5,408 Ìý
Investments
Ìý Ìý 3,768 Ìý Ìý Ìý 4,447 Ìý
Other assets
Ìý Ìý 431 Ìý Ìý Ìý 442 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total assets
Ìý $ 67,831 Ìý Ìý $ 87,430 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
LIABILITIES, SERIES D PREFERRED STOCK AND SHAREHOLDERSÂ’ EQUITY
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Current liabilities
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Accounts payable
Ìý $ 6,438 Ìý Ìý $ 4,784 Ìý
Accrued expenses
Ìý Ìý 5,342 Ìý Ìý Ìý 3,918 Ìý
Current portion of lines of credit
Ìý Ìý 8,564 Ìý Ìý Ìý 4,321 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total current liabilities
Ìý Ìý 20,344 Ìý Ìý Ìý 13,023 Ìý
Long-term interest payable to related party
Ìý Ìý — Ìý Ìý Ìý 3,409 Ìý
Deferred tax liabilities
Ìý Ìý 1,225 Ìý Ìý Ìý 1,339 Ìý
Line of credit with related party, net of unamortized discount of $0 and $68, respectively
Ìý Ìý — Ìý Ìý Ìý 11,932 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total liabilities
Ìý Ìý 21,569 Ìý Ìý Ìý 29,703 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Commitments and contingencies
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
SeriesÌýD Preferred stock — $0.01 par value, 2,000,000 shares authorized; 1,209,677 and 1,209,677 shares issued and outstanding (liquidation value of $32,413 and $30,613) at SeptemberÌý30, 2010 and DecemberÌý31, 2009, respectively
Ìý Ìý 26,128 Ìý Ìý Ìý 26,128 Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
ShareholdersÂ’ equity
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
SeriesÌýA Preferred stock — $0.01 par value, 4,000,000 shares authorized; 955,029 and 1,025,934 shares issued and outstanding (liquidation value of $2,566 and $2,564) at SeptemberÌý30, 2010 and DecemberÌý31, 2009, respectively
Ìý Ìý 10 Ìý Ìý Ìý 10 Ìý
SeriesÌýC Preferred Stock — $0.01 par value, 500,000 shares authorized; no shares issued or outstanding
Ìý Ìý — Ìý Ìý Ìý — Ìý
Common Stock — $0.01 par value, 500,000,000 shares authorized; 255,313,174 and 253,762,552 shares issued and outstanding at SeptemberÌý30, 2010 and DecemberÌý31, 2009, respectively
Ìý Ìý 2,553 Ìý Ìý Ìý 2,538 Ìý
Treasury stock - 45,154 shares at SeptemberÌý30, 2010 and DecemberÌý31, 2009, respectively
Ìý Ìý (61 ) Ìý Ìý (61 )
Additional paid-in capital
Ìý Ìý 373,146 Ìý Ìý Ìý 367,028 Ìý
Accumulated other comprehensive income
Ìý Ìý 2,149 Ìý Ìý Ìý 1,313 Ìý
Accumulated deficit
Ìý Ìý (357,663 ) Ìý Ìý (339,229 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total shareholdersÂ’ equity
Ìý Ìý 20,134 Ìý Ìý Ìý 31,599 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Total liabilities, Series D Preferred Stock and shareholdersÂ’ equity
Ìý $ 67,831 Ìý Ìý $ 87,430 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

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СÖíÊÓƵapp Health, Inc. and Subsidiaries
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited)
(in thousands, except share data)
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý For the three months ended Ìý Ìý For the nine months ended Ìý
Ìý Ìý September 30, Ìý Ìý September 30, Ìý
Ìý Ìý 2010 Ìý Ìý 2009 Ìý Ìý 2010 Ìý Ìý 2009 Ìý
Ìý Ìý Ìý Ìý Ìý (restated, Refer to NoteÌý12) Ìý Ìý Ìý Ìý Ìý (restated, Refer to NoteÌý12) Ìý
Revenue
Ìý $ 7,599 Ìý Ìý $ 1,501 Ìý Ìý $ 22,976 Ìý Ìý $ 6,149 Ìý
Cost of goods sold, excluding amortization of intangible assets
Ìý Ìý 5,255 Ìý Ìý Ìý 1,055 Ìý Ìý Ìý 15,633 Ìý Ìý Ìý 4,380 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Gross margin, excluding amortization of intangible assets
Ìý Ìý 2,344 Ìý Ìý Ìý 446 Ìý Ìý Ìý 7,343 Ìý Ìý Ìý 1,769 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Operating expenses
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Selling, general and administrative
Ìý Ìý 6,017 Ìý Ìý Ìý 3,089 Ìý Ìý Ìý 15,904 Ìý Ìý Ìý 9,272 Ìý
Research and development
Ìý Ìý 2,098 Ìý Ìý Ìý 2,805 Ìý Ìý Ìý 5,001 Ìý Ìý Ìý 10,962 Ìý
Other operating expenses, principally amortization of intangible assets
Ìý Ìý 973 Ìý Ìý Ìý 406 Ìý Ìý Ìý 2,775 Ìý Ìý Ìý 1,218 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Total operating expenses
Ìý Ìý 9,088 Ìý Ìý Ìý 6,300 Ìý Ìý Ìý 23,680 Ìý Ìý Ìý 21,452 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Operating loss
Ìý Ìý (6,744 ) Ìý Ìý (5,854 ) Ìý Ìý (16,337 ) Ìý Ìý (19,683 )
Other income (expense), net
Ìý Ìý (320 ) Ìý Ìý (458 ) Ìý Ìý (1,050 ) Ìý Ìý (1,402 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Loss before income taxes and investment loss
Ìý Ìý (7,064 ) Ìý Ìý (6,312 ) Ìý Ìý (17,387 ) Ìý Ìý (21,085 )
Income tax provision (benefit)
Ìý Ìý 82 Ìý Ìý Ìý (23 ) Ìý Ìý 183 Ìý Ìý Ìý (161 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Loss before investment loss in investee
Ìý Ìý (7,146 ) Ìý Ìý (6,289 ) Ìý Ìý (17,570 ) Ìý Ìý (20,924 )
Loss from investment in investee
Ìý Ìý (208 ) Ìý Ìý (65 ) Ìý Ìý (683 ) Ìý Ìý (103 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Net loss
Ìý Ìý (7,354 ) Ìý Ìý (6,354 ) Ìý Ìý (18,253 ) Ìý Ìý (21,027 )
Preferred stock dividend
Ìý Ìý (656 ) Ìý Ìý (3,944 ) Ìý Ìý (1,979 ) Ìý Ìý (4,060 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Net loss attributable to common shareholders
Ìý $ (8,010 ) Ìý $ (10,298 ) Ìý $ (20,232 ) Ìý $ (25,087 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Loss per common share, basic and diluted
Ìý $ (0.03 ) Ìý $ (0.04 ) Ìý $ (0.08 ) Ìý $ (0.11 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Weighted average number of common shares outstanding, basic and diluted
Ìý Ìý 255,307,381 Ìý Ìý Ìý 252,986,149 Ìý Ìý Ìý 255,007,220 Ìý Ìý Ìý 226,273,290 Ìý
The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

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СÖíÊÓƵapp Health, Inc. and Subsidiaries
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(unaudited)
(in thousands)
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý For the nine months ended Ìý
Ìý Ìý September 30, Ìý
Ìý Ìý 2010 Ìý Ìý 2009 Ìý
Cash flows from operating activities
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Net loss
Ìý $ (18,253 ) Ìý $ (21,027 )
Adjustments to reconcile net loss to net cash used in operating activities:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Depreciation and amortization
Ìý Ìý 3,043 Ìý Ìý Ìý 1,401 Ìý
Accretion of debt discount related to notes payable
Ìý Ìý 248 Ìý Ìý Ìý 49 Ìý
Share based compensation
Ìý Ìý 4,105 Ìý Ìý Ìý 3,536 Ìý
Provision for bad debts
Ìý Ìý 453 Ìý Ìý Ìý 58 Ìý
Provision for inventory obsolescence
Ìý Ìý 137 Ìý Ìý Ìý 80 Ìý
Loss from investment in investee
Ìý Ìý 683 Ìý Ìý Ìý 103 Ìý
Changes in:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Accounts receivable
Ìý Ìý (3,566 ) Ìý Ìý (448 )
Inventory
Ìý Ìý (2,473 ) Ìý Ìý (1,464 )
Prepaid expenses and other current assets
Ìý Ìý (50 ) Ìý Ìý 184 Ìý
Other assets
Ìý Ìý 270 Ìý Ìý Ìý (167 )
Accounts payable
Ìý Ìý 1,119 Ìý Ìý Ìý (968 )
Accrued expenses
Ìý Ìý (2,872 ) Ìý Ìý (1,382 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Net cash used in operating activities
Ìý Ìý (17,156 ) Ìý Ìý (20,045 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Cash flows from investing activities
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Acquisition of business, net of cash
Ìý Ìý (1,323 ) Ìý Ìý — Ìý
Investment in investee
Ìý Ìý — Ìý Ìý Ìý (4,800 )
Purchase of short-term marketable securities
Ìý Ìý (14,997 ) Ìý Ìý (9,997 )
Maturities of short-term marketable securities
Ìý Ìý 14,997 Ìý Ìý Ìý 4,997 Ìý
Capital expenditures
Ìý Ìý (630 ) Ìý Ìý (75 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Net cash used in investing activities
Ìý Ìý (1,953 ) Ìý Ìý (9,875 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Cash flows from financing activities:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Issuance of common stock for cash, to related parties
Ìý Ìý — Ìý Ìý Ìý 25,000 Ìý
Issuance of common stock for cash
Ìý Ìý — Ìý Ìý Ìý 25,990 Ìý
Issuance of SeriesÌýD preferred stock and warrants for cash, including related parties
Ìý Ìý — Ìý Ìý Ìý 30,000 Ìý
Repayment of line of credit with related party
Ìý Ìý (12,000 ) Ìý Ìý — Ìý
Borrowings under lines of credit
Ìý Ìý 5,476 Ìý Ìý Ìý — Ìý
Repayments under lines of credit
Ìý Ìý (1,875 ) Ìý Ìý — Ìý
Proceeds from bridge loan with related party
Ìý Ìý — Ìý Ìý Ìý 3,000 Ìý
Repayment of bridge loan with related party
Ìý Ìý — Ìý Ìý Ìý (3,000 )
Insurance financing
Ìý Ìý — Ìý Ìý Ìý 217 Ìý
Proceeds from the exercise of stock options and warrants
Ìý Ìý 27 Ìý Ìý Ìý 716 Ìý
Repayments of notes payable and capital lease obligations
Ìý Ìý — Ìý Ìý Ìý (290 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Net cash (used in) provided by financing activities
Ìý Ìý (8,372 ) Ìý Ìý 81,633 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Net (decrease)Ìýincrease in cash and cash equivalents
Ìý Ìý (27,481 ) Ìý Ìý 51,713 Ìý
Cash and cash equivalents at beginning of period
Ìý Ìý 42,658 Ìý Ìý Ìý 6,678 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Cash and cash equivalents at end of period
Ìý $ 15,177 Ìý Ìý $ 58,391 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
SUPPLEMENTAL INFORMATION
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Interest paid
Ìý $ 4,226 Ìý Ìý $ 51 Ìý
Income taxes refunded, net
Ìý $ (160 ) Ìý $ — Ìý
NON-CASH INVESTING AND FINANCING ACTIVITES
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Issuance of capital stock to acquire Pharmacos Exakta
Ìý $ 2,000 Ìý Ìý $ — Ìý
The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

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СÖíÊÓƵapp Health, Inc. and Subsidiaries
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)
NOTE 1 BUSINESS AND ORGANIZATION
ÌýÌýÌýÌýÌýWe are a specialty healthcare company involved in the discovery, development, and commercialization of pharmaceutical products, medical devices, vaccines, diagnostic technologies, and imaging systems. Initially focused on the treatment and management of ophthalmic diseases, we have since expanded into other areas of major unmet medical need. We are a Delaware corporation, headquartered in Miami, Florida.
NOTE 2 SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
ÌýÌýÌýÌýÌýBasis of presentation. The accompanying unaudited interim condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States and with the instructions to Form 10-Q and ArticleÌý10 of RegulationÌýS-X. Accordingly, they do not include all information and footnotes required by accounting principles generally accepted in the United States for complete financial statements. In the opinion of management, all adjustments (consisting of only normal recurring adjustments) considered necessary to present fairly the CompanyÂ’s results of operations, financial position and cash flows have been made. The results of operations and cash flows for the three and nine months ended SeptemberÌý30, 2010, are not necessarily indicative of the results of operations and cash flows that may be reported for the remainder of 2010 or for future periods. The interim condensed consolidated financial statements should be read in conjunction with the Consolidated Financial Statements and the Notes to Consolidated Financial Statements included in our Annual Report on Form 10-K for the year ended DecemberÌý31, 2009.
ÌýÌýÌýÌýÌýPrinciples of consolidation. The accompanying unaudited condensed consolidated financial statements include the accounts of СÖíÊÓƵapp Health, Inc. and our wholly-owned subsidiaries. All significant intercompany accounts and transactions are eliminated in consolidation.
ÌýÌýÌýÌýÌýUse of estimates. The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates.
ÌýÌýÌýÌýÌýComprehensive loss. Our comprehensive loss for the three and nine months ended SeptemberÌý30, 2010 includes net loss for the three and nine months and the cumulative translation adjustment, net of taxes of $0.8 million and $2.3 million, respectively, for the translation of the results of our subsidiaries in Chile and Mexico. Comprehensive loss for the three and nine months ended SeptemberÌý30, 2009 is comprised entirely of our net loss.
ÌýÌýÌýÌýÌýRevenue recognition. Generally, we recognize revenue from product sales when goods are shipped and title and risk of loss transfer to our customers. Certain of our instrumentation products are sold directly to end-users and require that we deliver, install and train the staff at the end-usersÂ’ facility. As a result, we do not recognize revenue until the product is delivered, installed and training has occurred.
ÌýÌýÌýÌýÌýDerivative financial instruments. We record derivative financial instruments on our balance sheet at their fair value and the changes in the fair value are recognized in income when they occur, the only exception being derivatives that qualify as hedges. To qualify the derivative instrument as a hedge, we are required to meet strict hedge effectiveness and contemporaneous documentation requirements at the initiation of the hedge and assess the hedge effectiveness on an ongoing basis over the life of the hedge. At SeptemberÌý30, 2010 and DecemberÌý31, 2009, our forward contracts for inventory purchases did not meet the documentation requirements to be designated as hedges. Accordingly, we recognize all changes in fair values in income. Refer to Note 7.
ÌýÌýÌýÌýÌýProduct warranties. Product warranty expense is recorded concurrently with the recording of revenue for product sales. The costs of warranties are accounted for as a component of cost of sales. We estimate warranty costs based on our estimated historical experience and adjust for any known product reliability issues.
ÌýÌýÌýÌýÌýAllowance for doubtful accounts. We analyze accounts receivable and historical bad debt levels, customer credit worthiness and current economic trends when evaluating the adequacy of the allowance for doubtful accounts using the specific identification method. Our reported net loss is directly affected by our estimate of the collectability of accounts receivable. Estimated allowances for sales returns are based upon our history of product returns. The

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amount of allowance for doubtful accounts at SeptemberÌý30, 2010 and DecemberÌý31, 2009, was $1.1Ìýmillion and $0.4Ìýmillion, respectively.
ÌýÌýÌýÌýÌýSegment reporting. Our chief operating decision-maker (“CODM”) is comprised of our executive management with the oversight of our board of directors. Our CODM review our operating results and operating plans and make resource allocation decisions on a company-wide or aggregate basis. We currently manage our operations in two reportable segments, pharmaceutical and instrumentation segments. The pharmaceutical segment consists of two operating segments, our (i)Ìýpharmaceutical research and development segment which is focused on the research and development of pharmaceutical products, diagnostic tests and vaccines, and (ii)Ìýthe pharmaceutical operations we acquired in Chile and Mexico through the acquisition of Pharma Genexx S.A. (“СÖíÊÓƵapp Chile”) and Pharmacos Exakta S.A. de C.V. (“Exakta-СÖíÊÓƵapp”). The instrumentation segment consists of ophthalmic instrumentation products and the activities related to the research, development, manufacture and commercialization of those products. There are no inter-segment sales. We evaluate the performance of each segment based on operating profit or loss. There is no inter-segment allocation of interest expense and income taxes.
ÌýÌýÌýÌýÌýEquity-based compensation. We measure the cost of employee services received in exchange for an award of equity instruments based on the grant-date fair value of the award. That cost is recognized in the statement of operations over the period during which an employee is required to provide service in exchange for the award. We record excess tax benefits, realized from the exercise of stock options as a financing cash inflow rather than as a reduction of taxes paid in cash flow from operations. Equity-based compensation arrangements to non-employees are recorded at their fair value on the measurement date. The measurement of equity-based compensation is subject to periodic adjustment as the underlying equity instruments vest. During the three months ended SeptemberÌý30, 2010 and 2009, we recorded $1.4Ìýmillion and $1.8Ìýmillion, respectively, of equity-based compensation expense. For the nine month period ending SeptemberÌý30, 2010 and 2009, we recorded $4.1Ìýmillion, and $3.5Ìýmillion, respectively, of equity-based compensation expense.
ÌýÌýÌýÌýÌýRecent accounting pronouncements. In MarchÌý2010, the Financial Accounting Standards Board, or FASB, issued updated guidance to amend and clarify how entities should evaluate credit derivatives embedded in beneficial interests in securitized financial assets. The updated guidance eliminates the scope exception for bifurcation of embedded credit derivatives in interests in securitized financial assets, unless they are created solely by subordination of one financial instrument to another. The update allows entities to elect the fair value option for any beneficial interest in securitized financial assets upon adoption. This guidance is effective by the first day of the first fiscal quarter beginning after JuneÌý15, 2010. Early adoption is permitted. We have not adopted this guidance early and are currently evaluating the potential effect of the adoption of this amendment on our results of operation and financial condition.
ÌýÌýÌýÌýÌýIn MarchÌý2010, the FASB reached a consensus to issue an amendment to the accounting for revenue arrangements under which a vendor satisfies its performance obligations to a customer over a period of time, when the deliverable or unit of accounting is not within the scope of other authoritative literature and when the arrangement consideration is contingent upon the achievement of a milestone. The amendment defines a milestone and clarifies whether an entity may recognize consideration earned from the achievement of a milestone in the period in which the milestone is achieved. This amendment is effective for fiscal years beginning on or after JuneÌý15, 2010, with early adoption permitted. The amendment may be applied retrospectively to all arrangements or prospectively for milestones achieved after the effective date. We have not adopted this guidance early and adoption of this amendment is not expected to have a material impact on our results of operation or financial condition.
ÌýÌýÌýÌýÌýIn JanuaryÌý2010, the FASB issued an amendment to the accounting for fair value measurements and disclosures. This amendment details additional disclosures on fair value measurements, requires a gross presentation of activities within a Level 3 rollforward and adds a new requirement to the disclosure of transfers in and out of Level 1 and Level 2 measurements. The new disclosures are required of all entities that are required to provide disclosures about recurring and nonrecurring fair value measurements. This amendment was effective as of JanuaryÌý1, 2010, with an exception for the gross presentation of Level 3 rollforward information, which is required for annual reporting periods beginning after DecemberÌý15, 2010, and for interim reporting periods within those years. The adoption of the remaining provisions of this amendment is not expected to have a material impact on our financial statement disclosures.
ÌýÌýÌýÌýÌýIn OctoberÌý2009, the FASB issued an amendment to the accounting for multiple-deliverable revenue arrangements. This amendment provides guidance on determining whether multiple deliverables exist, how the arrangements should be separated and how the consideration paid should be allocated. As a result of this

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amendment, entities may be able to separate multiple-deliverable arrangements in more circumstances than under existing accounting guidance. This guidance amends the requirement to establish the fair value of undelivered products and services based on objective evidence and instead provides for separate revenue recognition based upon managementÂ’s best estimate of the selling price for an undelivered item when there is no other means to determine the fair value of that undelivered item. The existing guidance previously required that the fair value of the undelivered item reflect the price of the item either sold in a separate transaction between unrelated third parties or the price charged for each item when the item is sold separately by the vendor. If the fair value of all of the elements in the arrangement was not determinable, then revenue was deferred until all of the items were delivered or fair value was determined. This amendment will be effective prospectively for revenue arrangements entered into or materially modified in fiscal years beginning on or after JuneÌý15, 2010. Early adoption and retrospective application is also permitted. We have not adopted this guidance early and are currently evaluating the potential effect of the adoption of this amendment on our results of operations and financial condition.
NOTE 3 LOSS PER SHARE
ÌýÌýÌýÌýÌýBasic loss per share is computed by dividing our net loss attributable to common shareholders by the weighted average number of shares outstanding during the period. Diluted earnings per share is computed by dividing our net loss attributable to common shareholders by the weighted average number of shares outstanding and the impact of all dilutive potential common shares, primarily stock options. The dilutive impact of stock options and warrants are determined by applying the “treasury stock” method.
ÌýÌýÌýÌýÌýA total of 20,968,349 and 20,998,353 potential common shares have been excluded from the calculation of net loss per share for the three months ended SeptemberÌý30, 2010 and 2009, respectively, because their inclusion would be anti-dilutive. A total of 20,067,981 and 17,154,864 potential common shares have been excluded from the calculation of net loss per share for the nine months ended SeptemberÌý30, 2010 and 2009, respectively, because their inclusion would be anti-dilutive. As of SeptemberÌý30, 2010, the holders of our SeriesÌýA Preferred Stock and SeriesÌýD Preferred Stock could convert their Preferred Shares into approximately 1,026,656 and 13,069,888 shares of our Common Stock, respectively.
NOTE 4 COMPOSITION OF CERTAIN FINANCIAL STATEMENT CAPTIONS
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
(in thousands) Ìý September 30, 2010 Ìý Ìý December 31, 2009 Ìý
Accounts receivable, net:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Accounts receivable
Ìý $ 14,589 Ìý Ìý $ 9,118 Ìý
Less allowance for doubtful accounts
Ìý Ìý (1,101 ) Ìý Ìý (351 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 13,488 Ìý Ìý $ 8,767 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Inventories, net:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Raw materials (including components for instrumentation)
Ìý $ 4,060 Ìý Ìý $ 3,764 Ìý
Work-in process
Ìý Ìý 1,085 Ìý Ìý Ìý 1,365 Ìý
Finished products
Ìý Ìý 9,248 Ìý Ìý Ìý 5,632 Ìý
Less provision for inventory reserve
Ìý Ìý (525 ) Ìý Ìý (241 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 13,868 Ìý Ìý $ 10,520 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Intangible assets, net:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Customer relationships
Ìý $ 7,527 Ìý Ìý $ 7,259 Ìý
Technology
Ìý Ìý 4,597 Ìý Ìý Ìý 4,597 Ìý
Product registrations
Ìý Ìý 4,090 Ìý Ìý Ìý 3,829 Ìý
Tradename
Ìý Ìý 651 Ìý Ìý Ìý 578 Ìý
Covenants not to compete
Ìý Ìý 365 Ìý Ìý Ìý 317 Ìý
Other
Ìý Ìý 7 Ìý Ìý Ìý 7 Ìý
Less amortization
Ìý Ìý (6,659 ) Ìý Ìý (3,865 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 10,578 Ìý Ìý $ 12,722 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
The change in value of the intangible assets reflects the foreign currency fluctuation between the Chilean peso and the US dollar at SeptemberÌý30, 2010 and DecemberÌý31, 2009.

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NOTE 5 ACQUISITION AND INVESTMENTS
ÌýÌýÌýÌýÌýOn FebruaryÌý17, 2010, we acquired Exakta-СÖíÊÓƵapp, a privately-owned Mexican company, engaged in the manufacture, marketing and distribution of ophthalmic and other pharmaceutical products for government and private markets since 1957. Pursuant to a purchase agreement we acquired all of the outstanding stock of Exakta-СÖíÊÓƵapp and real property owned by an affiliate of Exakta-СÖíÊÓƵapp for a total aggregate purchase price of $3.5Ìýmillion, of which an aggregate of $1.5Ìýmillion was paid in cash and $2.0Ìýmillion was paid in shares of our Common Stock, par value $.01. In SeptemberÌý2010, we reduced the consideration paid to the Sellers by $0.1Ìýmillion as Exakta-СÖíÊÓƵappÂ’s working capital was below the agreed upon minimum. The number of shares to be issued was determined by the average closing price of the CompanyÂ’s Common Stock as reported on the NYSE Amex for the ten trading days ending on FebruaryÌý12, 2010. A total of 1,372,428 shares of СÖíÊÓƵapp Common Stock were issued in the transaction which were valued at $2.0Ìýmillion due to trading restrictions. A portion of the proceeds will remain in escrow for a period of time to satisfy indemnification claims.
ÌýÌýÌýÌýÌýOn OctoberÌý1, 2009, we entered into a definitive agreement to acquire СÖíÊÓƵapp Chile, a privately-owned Chilean company engaged in the representation, importation, commercialization and distribution of pharmaceutical products, over-the-counter products and medical devices for government, private and institutional markets in Chile. Pursuant to a stock purchase agreement with СÖíÊÓƵapp Chile and its shareholders, Farmacias Ahumada S.A., FASA Chile S.A., and Laboratorios Volta S.A., we acquired all of the outstanding stock of СÖíÊÓƵapp Chile in exchange for $16Ìýmillion in cash. The transaction closed on OctoberÌý7, 2009.
ÌýÌýÌýÌýÌýEffective SeptemberÌý21, 2009, we entered into an agreement pursuant to which we invested $2.5 million in cash in Cocrystal Discovery, Inc., a privately held biopharmaceutical company (“Cocrystal”) in exchange for 1,701,723 shares of CocrystalÂ’s Convertible SeriesÌýA Preferred Stock. As of SeptemberÌý30, 2010, we own approximately 16% of CocrystalÂ’s outstanding stock.
ÌýÌýÌýÌýÌýWe have determined that Cocrystal has insufficient resources to carry out its principal activities without additional subordinated financial support. As such, Cocrystal meets the definition of a variable interest entity (“VIE”). In order to determine the primary beneficiary of the variable interest entity (“VIE”), we evaluated the related party group to identify who had the most significant power to control Cocrystal. Members of The Frost Group, LLC (the “Frost Group”) own approximately 4,422,967 shares, representing 42% of CocrystalÂ’s voting stock on an as converted basis, including 4,152,386 held by the Frost Gamma Investments Trust (the “Gamma Trust”). The Frost Group members include a trust controlled by Dr.ÌýFrost, who is our Chief Executive Officer and Chairman of the Board of Directors, Dr.ÌýJane H. Hsiao, who is the Vice Chairman of the Board of Directors and Chief Technical Officer, Steven D. Rubin who is Executive Vice President - Administration and a director of the Company and Rao Uppaluri who is our Chief Financial Officer. Dr.ÌýFrost, Mr.ÌýRubin, and Dr.ÌýHsiao currently serve on the Board of Directors of Cocrystal and represent 50% of its board. In addition, the Gamma Trust influenced the redesign of Cocrystal and can significantly influence the success of Cocrystal through its board representation and voting power. As such, we have determined that the Gamma Trust is the primary beneficiary within the related party group. As a result of our determination that we are not the primary beneficiary, we have accounted for our investment in Cocrystal under the equity method.
ÌýÌýÌýÌýÌýOn JuneÌý10, 2009, we entered into a stock purchase agreement with Sorrento Therapeutics, Inc. (“Sorrento”), a company with a technology for generating fully human monoclonal antibodies, pursuant to which we invested $2.3Ìýmillion in Sorrento. We own approximately 53,113,732 shares of Sorrento common stock, or approximately 24% of SorrentoÂ’s total outstanding common stock at SeptemberÌý30, 2010. The closing stock price for SorrentoÂ’s common stock, a thinly traded stock, as quoted on the over-the-counter markets was $1.75 per share on SeptemberÌý30, 2010. We account for our investment in Sorrento under the equity method.
NOTE 6 FAIR VALUE MEASUREMENTS
ÌýÌýÌýÌýÌýWe record fair value at an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or liability. We utilize a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value. These tiers include: Level 1, defined as observable inputs such as quoted prices in active markets; Level 2, defined as inputs other than quoted prices in active markets that are either directly or indirectly observable; and Level 3, defined as unobservable inputs in which little or no market data exists, therefore requiring an entity to develop its own assumptions.

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ÌýÌýÌýÌýÌýAs of SeptemberÌý30, 2010, we held money market funds that qualify as cash equivalents and forward contracts for inventory purchases that are required to be measured at fair value on a recurring basis. Refer to Note 7. The carrying values of our other assets and liabilities approximate their fair value due to their short-term nature.
ÌýÌýÌýÌýÌýUpon the termination of an employee of Ophthalmics Technologies, Inc., or OTI, we became obligated at the former employeeÂ’s sole option to acquire up to 10% of the shares issued to the employee in connection with the acquisition of OTI at a price of $3.55 per share. In February 2009, this employee exercised his put option and we repurchased 27,154 shares of our Common Stock at $3.55 per share for a total of $0.1Ìýmillion. In addition, an existing employee of OTI has the same provision within his employment arrangement with a potential obligation of approximately $0.3Ìýmillion. We have recorded approximately $0.1Ìýmillion and $0.2Ìýmillion in accrued expenses as of SeptemberÌý30, 2010 and DecemberÌý31, 2009, respectively, based on the estimated fair value of the unexercised put option.
ÌýÌýÌýÌýÌýThe OTI put options were valued at fair value utilizing the Black-Scholes-Merton valuation method. During the three months ended SeptemberÌý30, 2010 and 2009, we recorded a reversal of expense of $6 thousand and $35 thousand, respectively, reflecting our stock price fluctuations. During the nine months ended SeptemberÌý30, 2010 and 2009, we recorded a reversal of expense of $46 thousand and $0.1Ìýmillion, respectively, reflecting our stock price fluctuations.
ÌýÌýÌýÌýÌýAny future fluctuation in fair value related to these instruments that is judged to be temporary, including any recoveries of previous write-downs, would be recorded in accumulated other comprehensive income or loss. If we determine that any future valuation adjustment was other-than-temporary, we would record a charge to the consolidated statement of operations as appropriate.
ÌýÌýÌýÌýÌýOur financial assets and liabilities measured at fair value on a recurring basis are as follows:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý Fair value measurements as of September 30, 2010 Ìý
Ìý Ìý Quoted prices in Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý active markets for Ìý Ìý Significant other Ìý Ìý Significant Ìý Ìý Ìý Ìý
Ìý Ìý identical assets Ìý Ìý observable inputs Ìý Ìý unobservable inputs Ìý Ìý Ìý Ìý
(in thousands) Ìý (Level 1) Ìý Ìý (Level 2) Ìý Ìý (Level 3) Ìý Ìý Total Ìý
Assets:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Money market funds
Ìý $ 13,976 Ìý Ìý $ — Ìý Ìý $ — Ìý Ìý $ 13,976 Ìý
Forward contracts
Ìý Ìý — Ìý Ìý Ìý 620 Ìý Ìý Ìý — Ìý Ìý Ìý 620 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Total assets
Ìý $ 13,976 Ìý Ìý $ 620 Ìý Ìý $ — Ìý Ìý $ 14,596 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Liabilities:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
OTI put option
Ìý $ — Ìý Ìý $ 130 Ìý Ìý $ — Ìý Ìý $ 130 Ìý
NOTE 7 DERIVATIVE CONTRACTS
ÌýÌýÌýÌýÌýWe enter into foreign currency forward exchange contracts to cover the risk of exposure to exchange rate differences arising from inventory purchases on letters of credit. Under these forward contracts, for any rate above or below the fixed rate, we receive or pay the difference between the spot rate and the fixed rate for the given amount at the settlement date.
ÌýÌýÌýÌýÌýWe record derivative financial instruments on our balance sheet at their fair value as an accrued expense and the changes in the fair value are recognized in income in other expense net when they occur, the only exception being derivatives that qualify as hedges. To qualify the derivative instrument as a hedge, we are required to meet strict hedge effectiveness and contemporaneous documentation requirements at the initiation of the hedge and assess the hedge effectiveness on an ongoing basis over the life of the hedge. At SeptemberÌý30, 2010, the forward contracts did not meet the documentation requirements to be designated as hedges. Accordingly, we recognize all changes in fair values in income.

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ÌýÌýÌýÌýÌýThe outstanding contracts at SeptemberÌý30, 2010, have been recorded at fair value, and their maturity details are as follows:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
(in thousands) Ìý Ìý Ìý Ìý Ìý Fair value at Ìý Ìý Unrealized gain Ìý
Days until maturity Ìý Contract value Ìý Ìý September 30, 2010 Ìý Ìý (loss) Ìý
0 to 30
Ìý $ 786 Ìý Ìý $ 842 Ìý Ìý $ 56 Ìý
31 to 60
Ìý Ìý 461 Ìý Ìý Ìý 484 Ìý Ìý Ìý 23 Ìý
61 to 90
Ìý Ìý 1,471 Ìý Ìý Ìý 1,560 Ìý Ìý Ìý 89 Ìý
91 to 120
Ìý Ìý 214 Ìý Ìý Ìý 228 Ìý Ìý Ìý 14 Ìý
121 to 180
Ìý Ìý 2,181 Ìý Ìý Ìý 2,338 Ìý Ìý Ìý 157 Ìý
More than 180
Ìý Ìý 2,915 Ìý Ìý Ìý 3,196 Ìý Ìý Ìý 281 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Total
Ìý $ 8,028 Ìý Ìý $ 8,648 Ìý Ìý $ 620 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
NOTE 8 RELATED PARTY TRANSACTIONS
ÌýÌýÌýÌýÌýOn JulyÌý20, 2010, we entered into a use agreement for approximately 1,100 square feet of space in Jupiter, Florida to house our molecular diagnostics operations from The Scripps Research Institute (“Scripps”). Dr.ÌýFrost is a member of the Board of Trustees of Scripps and Dr.ÌýRichard Lerner, a member of our Board of Directors, is also the President of Scripps. Pursuant to the terms of the use agreement, which is effective as of NovemberÌý1, 2009, gross rent is approximately $40 thousand per year for a two-year term which may be extended, upon mutual agreement, for one additional year.
ÌýÌýÌýÌýÌýOn JuneÌý1, 2010, the Company entered into a cooperative research and development agreement with Academia Sinica in Taipei, Taiwan, for pre-clinical work for a compound against various forms of cancer. Dr.ÌýAlice Yu, a member of our board of directors, is a Distinguished Research Fellow and Associate Director at the Genomics Research Center, Academia Sinica. In connection with the agreement, we are required to pay Academia Sinica approximately $0.2Ìýmillion over the term of the agreement.
ÌýÌýÌýÌýÌýEffective MarchÌý5, 2010, the Frost Group assigned two license agreements with Academia Sinica to the CompanyÂ’s subsidiary, СÖíÊÓƵapp Taiwan, Inc. The license agreements pertain to alpha-galactosyl ceramide analogs and their use as immunotherapies and peptide ligands in the diagnosis and treatment of cancer. In connection with the assignment of the two licenses, the Company agreed to reimburse the Frost Group for the licensing fees previously paid by the Frost Group to Academia Sinica in the amounts of $50 thousand and $75 thousand, respectively, as well as reimbursement of certain expenses of $50 thousand.
ÌýÌýÌýÌýÌýEffective SeptemberÌý21, 2009, we entered into an agreement pursuant to which we invested $2.5Ìýmillion in Cocrystal in exchange for 1,701,723 shares of CocrystalÂ’s Convertible SeriesÌýA Preferred Stock. A group of Investors, led by the Frost Group (the “Cocrystal Investors”), previously invested $5Ìýmillion in Cocrystal, and agreed to invest an additional $5Ìýmillion payable in two equal installments in SeptemberÌý2009 and MarchÌý2010. As a result of an amendment to the Cocrystal Investors agreements dated JuneÌý9, 2009, СÖíÊÓƵapp, rather than the Cocrystal Investors, made the first installment investment ($2.5Ìýmillion) on SeptemberÌý21, 2009. Refer to Note 5.
ÌýÌýÌýÌýÌýOn JulyÌý20, 2009, the Company entered into a worldwide exclusive license agreement with Academia Sinica in Taipei, Taiwan, for a new technology to develop protein vaccines against influenza and other viral infections. Dr.ÌýAlice Yu, a member of our Board of Directors, is a Distinguished Research Fellow and Associate Director at the Genomics Research Center, Academia Sinica.
ÌýÌýÌýÌýÌýOn JuneÌý16, 2009, we entered into an agreement to lease approximately 10,000 square feet of space in Hialeah, Florida to house manufacturing and service operations for our ophthalmic instrumentation business (the “Hialeah Facility”) from an entity controlled by Dr.ÌýFrost and Dr. Jane Hsiao. Pursuant to the terms of a lease agreement, which is effective as of FebruaryÌý1, 2009, gross rent is $0.1Ìýmillion per year for a one-year lease which was extended, for one additional year. From AprilÌý2008 through JanuaryÌý2009, we leased 20,000 square feet at the Hialeah Facility from a third party landlord pursuant to a lease agreement which contained an option to purchase the facility. We initially elected to exercise the option to purchase the Hialeah Facility in SeptemberÌý2008. Prior to closing, however, we assigned the right to purchase the Hialeah Facility to an entity controlled by Drs.ÌýFrost and Hsiao and leased a smaller portion of the facility as a result of several factors, including our inability to obtain outside financing for the purchase, current business needs, the reduced operating costs for the smaller space and the minimization of risk and expense of unutilized space.

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ÌýÌýÌýÌýÌýIn MarchÌý2009, we paid the $45 thousand filing fee to the Federal Trade Commission in connection with filings made by us and Dr.ÌýFrost, under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 (“HSR”). The filings permitted Dr.ÌýFrost and his affiliates to acquire additional shares of our Common Stock upon expiration of the HSR waiting period on MarchÌý23, 2009.
ÌýÌýÌýÌýÌýIn NovemberÌý2007, we entered into an office lease with Frost Real Estate Holdings, LLC, an entity affiliated with Dr.ÌýFrost. The lease is for approximately 8,300 square feet of space in an office building in Miami, Florida, where the CompanyÂ’s principal executive offices are located. We had previously been leasing this space from Frost Real Estate Holdings on a month-to-month basis while the parties were negotiating the lease. The lease provides for payments of approximately $18 thousand per month in the first year increasing annually to $24 thousand per month in the fifth year, plus applicable sales tax. The rent is inclusive of operating expenses, property taxes and parking. The rent for the first year was reduced to reflect a $30 thousand credit for the costs of tenant improvements. From JanuaryÌý1, 2008 through OctoberÌý1, 2008, we leased an additional 1,100 square feet of general office and laboratory space on a ground floor annex of our corporate office building pursuant to an addendum to the Lease, which required us to pay annual rent of $19 thousand per year for the annex space.
ÌýÌýÌýÌýÌýOn SeptemberÌý19, 2007, we entered into an exclusive technology license agreement with Winston Laboratories, Inc. (“Winston”) pursuant to which we acquired an exclusive license to the proprietary rights of certain products in exchange for the payment of an initial licensing fee, royalties, and payments on the occurrence of certain milestones. On FebruaryÌý23, 2010, we provided Winston notice of termination of the license agreement, and the agreement terminated on MayÌý24, 2010. Previously, members of the Frost Group, LLC, or the Frost Group, beneficially owned approximately 30% of Winston Pharmaceuticals, Inc., and Dr. Uppaluri, our Chief Financial Officer, served as a member of WinstonÂ’s board. Effective MayÌý19, 2010, the members of the Frost Group sold 100% of WinstonÂ’s capital stock beneficially owned by them (consisting of an aggregate of 18,399,271 outstanding shares of common stock and warrants to purchase an aggregate of 8,958,975 shares of common stock) to an entity whose members include Dr. Joel E. Bernstein, the President and Chief Executive Officer of Winston. As consideration for the sale, the Frost Group members received an aggregate of $789,500 in cash and non-recourse promissory notes in the aggregate principal amount of $10,263,500 (the “Promissory Notes”). Dr.ÌýUppaluri resigned from the Winston board effective MayÌý19, 2010.
ÌýÌýÌýÌýÌýWe have a $12.0Ìýmillion line of credit with the Frost Group, a related party. On JuneÌý2, 2010 we repaid all amounts outstanding on the line of credit including $12Ìýmillion in principal and $4.1 million in interest. We have the ability to redraw funds under the line of credit until its expiration in JanuaryÌý2011. We are obligated to pay interest upon maturity, capitalized quarterly, on outstanding borrowings under the line of credit at an 11% annual rate, which is due JanuaryÌý11, 2011. The line of credit is collateralized by all of our personal property except our intellectual property.
ÌýÌýÌýÌýÌýWe reimburse Dr.ÌýFrost for Company-related use by Dr.ÌýFrost and our other executives of an airplane owned by a company that is beneficially owned by Dr.ÌýFrost. We reimburse Dr.ÌýFrost in an amount equal to the cost of a first class airline ticket between the travel cities for each executive, including Dr.ÌýFrost, traveling on the airplane for Company-related business. We do not reimburse Dr.ÌýFrost for personal use of the airplane by Dr.ÌýFrost or any other executive; nor do we pay for any other fixed or variable operating costs of the airplane. For the three and nine months ended SeptemberÌý30, 2010, we reimbursed Dr.ÌýFrost approximately $5 thousand and $30 thousand, respectively, for Company-related travel by Dr.ÌýFrost and other СÖíÊÓƵapp executives. For the three and nine months ended SeptemberÌý30, 2009, we reimbursed Dr.ÌýFrost approximately $9 thousand and $55 thousand, respectively, for Company-related travel by Dr.ÌýFrost and other СÖíÊÓƵapp executives.
NOTE 9 COMMITMENTS AND CONTINGENCIES
ÌýÌýÌýÌýÌýOn JanuaryÌý7, 2010, we received a letter from counsel to Nidek Co., Ltd. (“Nidek”) alleging that Ophthalmic Technologies, Inc. (“OTI”) or СÖíÊÓƵapp breached its service obligations to Nidek under the Service Agreement between OTI, Nidek and Newport Corporation, dated DecemberÌý29, 2006, and the Service Agreement by and between Nidek and OTI, dated the same date. We have had discussions with Nidek regarding the matter, but it is too early to assess the likelihood of litigation in this matter or the probability of a favorable or unfavorable outcome. We do not believe this matter will have a material impact on our results of operations or financial condition. We are also assessing possible claims of indemnification against a supplier in connection with the matter.

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ÌýÌýÌýÌýÌýOn MayÌý6, 2008, we completed the acquisition of Vidus Ocular, Inc., or Vidus. Pursuant to a Securities Purchase Agreement with Vidus, each of its stockholders, and the holders of convertible promissory notes issued by Vidus, we acquired all of the outstanding stock and convertible debt of Vidus in exchange for (i)Ìýthe issuance and delivery at closing of 658,080 shares of our common stock (the “Closing Shares”); (ii)Ìýthe issuance of 488,420 shares of our common stock to be held in escrow pending the occurrence of certain development milestones (the “Milestone Shares”); and (iii)Ìýthe issuance of options to acquire 200,000 shares of our common stock. Additionally, in the event that the stock price for our common stock at the time of receipt of approval or clearance by the U.S. Food & Drug Administration of a pre-market notification 510(k) relating to the Aquashunt™ is not at or above a specified price, we will be obligated to issue an additional 413,850 shares of our common stock.
ÌýÌýÌýÌýÌýWe have a potential obligation of approximately $0.3Ìýmillion related to a put option held by an employee. Refer to Note 6.
ÌýÌýÌýÌýÌýWe expect to incur losses from operations for the foreseeable future. We expect to incur substantial research and development expenses, including expenses related to the hiring of personnel and additional clinical trials. We expect that selling, general and administrative expenses will also increase as we expand our sales, marketing and administrative staff and add infrastructure. We intend to finance additional research and development projects, clinical trials and our future operations with a combination of private placements, payments from potential strategic research and development, licensing and/or marketing arrangements, public offerings, debt financing and revenues from future product sales, if any. There can be no assurance, however, that additional capital will be available to us on acceptable terms, or at all.
ÌýÌýÌýÌýÌýWe are a party to other litigation in the ordinary course of business. We do not believe that any such other litigation will have a material adverse effect on our business, financial condition or results of operations.
NOTE 10 SEGMENTS
ÌýÌýÌýÌýÌýWe currently manage our operations in two reportable segments, pharmaceutical and instrumentation segments. The pharmaceutical segment consists of two operating segments, our (i) pharmaceutical research and development segment which is focused on the research and development of pharmaceutical products, diagnostic tests and vaccines, and (ii)Ìýthe pharmaceutical operations we acquired in Chile and Mexico through the acquisition of СÖíÊÓƵapp Chile and Exakta-СÖíÊÓƵapp. The instrumentation segment consists of ophthalmic instrumentation products and the activities related to the research, development, manufacture and commercialization of those products. There are no inter-segment sales. We evaluate the performance of each segment based on operating profit or loss. There is no inter-segment allocation of interest expense and income taxes.

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ÌýÌýÌýÌýÌýInformation regarding our operations and assets for the two segments and the unallocated corporate operations as well as geographic information are as follows:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý For the three months ended September 30, Ìý Ìý For the nine months ended September 30, Ìý
(in thousands) Ìý 2010 Ìý Ìý 2009 Ìý Ìý 2010 Ìý Ìý 2009 Ìý
Revenue
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Pharmaceutical
Ìý $ 5,677 Ìý Ìý $ — Ìý Ìý $ 16,262 Ìý Ìý $ — Ìý
Instrumentation
Ìý Ìý 1,922 Ìý Ìý Ìý 1,501 Ìý Ìý Ìý 6,714 Ìý Ìý Ìý 6,149 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 7,599 Ìý Ìý $ 1,501 Ìý Ìý $ 22,976 Ìý Ìý $ 6,149 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Operating loss
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Pharmaceutical
Ìý $ (1,310 ) Ìý $ (510 ) Ìý $ (3,369 ) Ìý $ (7,158 )
Instrumentation
Ìý Ìý (2,587 ) Ìý Ìý (1,790 ) Ìý Ìý (4,521 ) Ìý Ìý (3,779 )
Corporate
Ìý Ìý (2,847 ) Ìý Ìý (3,554 ) Ìý Ìý (8,447 ) Ìý Ìý (8,746 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ (6,744 ) Ìý $ (5,854 ) Ìý $ (16,337 ) Ìý $ (19,683 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Depreciation and amortization
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Pharmaceutical
Ìý $ 536 Ìý Ìý $ 10 Ìý Ìý $ 1,579 Ìý Ìý $ 23 Ìý
Instrumentation
Ìý Ìý 445 Ìý Ìý Ìý 447 Ìý Ìý Ìý 1,333 Ìý Ìý Ìý 1,338 Ìý
Corporate
Ìý Ìý 45 Ìý Ìý Ìý 9 Ìý Ìý Ìý 78 Ìý Ìý Ìý 40 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 1,026 Ìý Ìý $ 466 Ìý Ìý $ 2,990 Ìý Ìý $ 1,401 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Revenue
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
United States
Ìý $ 335 Ìý Ìý $ 233 Ìý Ìý $ 704 Ìý Ìý $ 474 Ìý
Chile
Ìý Ìý 4,517 Ìý Ìý Ìý — Ìý Ìý Ìý 13,711 Ìý Ìý Ìý — Ìý
Mexico
Ìý Ìý 1,200 Ìý Ìý Ìý — Ìý Ìý Ìý 2,591 Ìý Ìý Ìý — Ìý
All others
Ìý Ìý 1,547 Ìý Ìý Ìý 1,268 Ìý Ìý Ìý 5,790 Ìý Ìý Ìý 5,675 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 7,599 Ìý Ìý $ 1,501 Ìý Ìý $ 22,976 Ìý Ìý $ 6,149 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý As of Ìý
Ìý Ìý September 30, 2010 Ìý Ìý December 31, 2009 Ìý
Assets
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Pharmaceutical
Ìý $ 39,985 Ìý Ìý $ 28,813 Ìý
Instrumentation
Ìý Ìý 9,200 Ìý Ìý Ìý 12,262 Ìý
Corporate
Ìý Ìý 18,646 Ìý Ìý Ìý 46,355 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
Ìý $ 67,831 Ìý Ìý $ 87,430 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý
ÌýÌýÌýÌýÌýDuring the three months ended SeptemberÌý30, 2010, our largest customer represented approximately 12% of our total revenue. During the three months ended SeptemberÌý30, 2009, our two largest customers represented approximately 17%, and 10%, respectively, of our revenue. During the nine months ended SeptemberÌý30, 2010, our largest customer represented approximately 14% of our total revenue. During the nine months ended SeptemberÌý30, 2009, our three largest customers represented approximately 18%, 14%, and 12%, respectively, of our revenue. As of SeptemberÌý30, 2010, two customers represented approximately 29% and 11% of our accounts receivable balance, respectively. As of DecemberÌý31, 2009, two customers represented 32% and 19%, respectively, of our accounts receivable balance.
NOTE 11 SUBSEQUENT EVENTS
ÌýÌýÌýÌýÌýOn NovemberÌý1, 2010, we received notification from the U.S. Internal Revenue Service that we were awarded $0.7Ìýmillion in grants under section 48D of the internal revenue code for research and development expenses incurred during 2009 and 2010.
ÌýÌýÌýÌýÌýOn NovemberÌý3, 2010, we announced that we made an investment in Fabrus, LLC, a privately held early stage biotechnology company with next generation therapeutic antibody drug discovery and development capabilities. In exchange for the CompanyÂ’s investment, the Company acquired approximately 13% of FabrusÂ’ outstanding membership interests on a fully diluted basis for $0.7 million.
ÌýÌýÌýÌýÌýWe have reviewed all subsequent events and transactions that occurred after the date of our SeptemberÌý30, 2010 consolidated balance sheet date, through the time of filing this Quarterly Report on Form 10-Q on NovemberÌý9, 2010.
NOTE 12 RESTATEMENT OF FINANCIAL STATEMENTS
ÌýÌýÌýÌýÌýThe Company has restated its previously issued consolidated financial statements as of and for the quarter ended September 30, 2009, and as of and for the year ended December 31, 2009, to reflect the CompanyÂ’s determination that it did not properly account for the September 28, 2009 Series D Convertible Preferred Stock (the “Preferred Stock”) offering. In connection with the issuance of 1,209,667 shares of Preferred Stock, we issued warrants to purchase up to an aggregate of 3,024,194 shares of our Common Stock at an exercise price of $2.48 per share. The Company should have allocated the $30 million in proceeds received from the issuance of the Preferred Stock and warrants to those instruments based on their relative fair values, which would have resulted in a $3.9 million beneficial conversion feature. Because the Preferred Stock was immediately convertible into common stock, the beneficial conversion feature should have been immediately recognized as a deemed dividend and should have increased the loss attributable to common shareholders. In addition, the Company is correcting the classification of the Series D Convertible Preferred Stock from a component of equity to the mezzanine section of the balance sheet.

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ÌýÌýÌýÌýÌýThe CompanyÂ’s restated consolidated financial statements reflect the following changes:
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý December 31, 2009 Ìý
(in thousands) Ìý As reported Ìý Ìý Adjustment Ìý Ìý Restated Ìý
Total Liabilities
Ìý $ 29,703 Ìý Ìý $ — Ìý Ìý $ 29,703 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
SeriesÌýD Preferred Stock
Ìý Ìý — Ìý Ìý Ìý 26,128 Ìý Ìý Ìý 26,128 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý
ShareholdersÂ’ equity
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
SeriesÌýA Preferred Stock
Ìý Ìý 10 Ìý Ìý Ìý — Ìý Ìý Ìý 10 Ìý
SeriesÌýD Preferred Stock
Ìý Ìý 12 Ìý Ìý Ìý (12 ) Ìý Ìý — Ìý
Common Stock
Ìý Ìý 2,538 Ìý Ìý Ìý — Ìý Ìý Ìý 2,538 Ìý
Treasury Stock
Ìý Ìý (61 ) Ìý Ìý — Ìý Ìý Ìý (61 )
Additional paid-in capital
Ìý Ìý 393,144 Ìý Ìý Ìý (26,116 ) Ìý Ìý 367,028 Ìý
Accumulated deficit
Ìý Ìý (339,229 ) Ìý Ìý — Ìý Ìý Ìý (339,229 )
Cumulative translation adjustment
Ìý Ìý 1,313 Ìý Ìý Ìý — Ìý Ìý Ìý 1,313 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Total shareholdersÂ’ equity
Ìý Ìý 57,727 Ìý Ìý Ìý (26,128 ) Ìý Ìý 31,599 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Total liabilities, Series D Preferred Stock and shareholdersÂ’ equity
Ìý $ 87,430 Ìý Ìý $ — Ìý Ìý $ 87,430 Ìý
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Ìý Ìý For the three months ended September 30, 2009 Ìý Ìý For the nine months ended September 30, 2009 Ìý
(in thousands) Ìý As Reported Ìý Ìý Adjusted Ìý Ìý Restated Ìý Ìý As Reported Ìý Ìý Adjusted Ìý Ìý Restated Ìý
Net loss
Ìý $ (6,354 ) Ìý $ — Ìý Ìý $ (6,354 ) Ìý $ (21,027 ) Ìý $ — Ìý Ìý $ (21,027 )
Preferred stock dividend
Ìý Ìý (72 ) Ìý Ìý (3,872 ) Ìý Ìý (3,944 ) Ìý Ìý (188 ) Ìý Ìý (3,872 ) Ìý Ìý (4,060 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Net loss attributable to common shareholders
Ìý $ (6,426 ) Ìý Ìý (3,872 ) Ìý $ (10,298 ) Ìý $ (21,215 ) Ìý Ìý (3,872 ) Ìý $ (25,087 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Basic and diluted loss per share
Ìý $ (0.03 ) Ìý $ (0.02 ) Ìý $ (0.04 ) Ìý $ (0.09 ) Ìý $ (0.02 ) Ìý $ (0.11 )
Ìý
Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý Ìý
Weighted average number of common shares outstanding, basic and diluted
Ìý Ìý 252,986,149 Ìý Ìý Ìý Ìý Ìý Ìý Ìý 252,986,149 Ìý Ìý Ìý 226,273,290 Ìý Ìý Ìý Ìý Ìý Ìý Ìý 226,273,290 Ìý
ItemÌý2. ManagementÂ’s Discussion and Analysis of Financial Condition and Results of Operations
OVERVIEW
ÌýÌýÌýÌýÌýYou should read this discussion together with the condensed consolidated financial statements, related Notes, and other financial information included elsewhere in this report and in our Annual Report on Form 10-K for the year ended DecemberÌý31, 2009 (the “FormÌý10-K”). The following discussion contains assumptions, estimates and other forward-looking statements that involve a number of risks and uncertainties, including those discussed under “Risk Factors,” in PartÌýII, Item 1A of our Form 10-K for the year ended DecemberÌý31, 2009 and in other reports filed by us with the SEC. These risks could cause our actual results to differ materially from those anticipated in these forward-looking statements.
ÌýÌýÌýÌýÌýWe are a specialty healthcare company involved in the discovery, development and commercialization of pharmaceutical products, medical devices, vaccines, diagnostic technologies and imaging systems. Initially focused on the treatment and management of ophthalmic diseases, we have since expanded into other areas of major unmet medical need. To date, we have devoted a significant portion of our efforts towards research and development. As of SeptemberÌý30, 2010, we had an accumulated deficit of $357.6Ìýmillion. Since we do not generate revenue from any of our pharmaceutical product candidates and have only generated limited revenue from our pharmaceutical operations in Chile and Mexico and our instrumentation business, we expect to continue to generate significant losses in connection with the research and development activities relating to our product candidates and other technologies. Such research and development activities are budgeted to expand over time and will require further resources if we are to be successful. As a result, we believe that our operating losses are likely to be substantial over the next several years. We will need to obtain additional funds to further develop our research and development programs, and there can be no assurance that additional capital will be available to us on acceptable terms, or at all.
RESULTS OF OPERATIONS
FOR THE THREE MONTHS ENDED SEPTEMBER 30, 2010 AND 2009
ÌýÌýÌýÌýÌýRevenue. Revenue for the three months ended SeptemberÌý30, 2010, was $7.6Ìýmillion, compared to $1.5Ìýmillion for the comparable 2009 period. The increase in revenue during the three months ended SeptemberÌý30, 2010 is primarily due to revenue from our pharmaceutical businesses in Chile and Mexico, respectively. We acquired Pharma Genexx S.A., (“СÖíÊÓƵapp Chile”), in OctoberÌý2009 and Pharmacos Exakta S.A. de C.V. (“Exakta-СÖíÊÓƵapp”) in FebruaryÌý2010. As a result, the 2009 period reflects revenue only from our instrumentation business. Revenue from our instrumentation business increased from the 2009 period, as a result of increased demand for our OCT/SLO and ultrasound products in international markets.
ÌýÌýÌýÌýÌýGross margin. Gross margin for the three months ended SeptemberÌý30, 2010, was $2.3Ìýmillion compared to $0.4Ìýmillion for the comparable period of 2009. Gross margin for the three months ended SeptemberÌý30, 2010, increased from the 2009 period primarily as a result of the gross margin generated by our pharmaceutical business.
ÌýÌýÌýÌýÌýSelling, general and administrative expense. Selling, general and administrative expense for the three months ended SeptemberÌý30, 2010, was $6.0Ìýmillion compared to $3.1Ìýmillion of expense for the comparable period of 2009. The increase in selling, general and administrative expenses primarily reflects the increase in selling expenses related to our pharmaceutical business. Selling, general and administrative expenses during the three months ended SeptemberÌý30, 2010 and 2009, primarily include personnel expenses, including equity-based compensation expense of $1.2Ìýmillion and $0.8Ìýmillion, respectively, and professional fees.
ÌýÌýÌýÌýÌýResearch and development expense. Research and development expense during the three months ended SeptemberÌý30, 2010 and 2009, was $2.1Ìýmillion and $2.8Ìýmillion, respectively. The decrease for the three months ended SeptemberÌý30, 2010, primarily reflects decreased equity-based compensation expense and professional fees, partially offset by increased activities related to our rolapitant and molecular diagnostics development programs. Research and development expenses during the three months ended SeptemberÌý30, 2010, includes equity-based compensation expense of $0.2Ìýmillion, compared to $1.0Ìýmillion for the 2009 period.
ÌýÌýÌýÌýÌýOther operating expenses. Other operating expenses for the three months ended SeptemberÌý30, 2010, as compared to the three months ended SeptemberÌý30, 2009, increased by $0.6Ìýmillion primarily as a result of the amortization of the intangible assets recorded as part of the acquisition of СÖíÊÓƵapp Chile and also includes amortization of intangible assets recorded as part of the acquisitions of OTI and Exakta-СÖíÊÓƵapp. The 2009 period only includes the amortization expense of the intangible assets acquired from OTI.

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ÌýÌýÌýÌýÌýOther income and expenses, net. Other income and expense, net was $0.3Ìýmillion for the three months ended SeptemberÌý30, 2010 compared to other income and expense, net of $0.5Ìýmillion for the comparable 2009 period. Other income primarily consists of interest earned on our cash and cash equivalents and other expense primarily includes foreign currency expense during the 2010 period. Other expense during the 2009 period primarily reflects the interest incurred on our line of credit with The Frost Group LLC (the “Frost Group”). On JuneÌý2, 2010, we repaid all amounts outstanding on the Frost Group line of credit including $12Ìýmillion in principal and $4.1Ìýmillion in interest. We have the ability to redraw funds under the line of credit until its expiration in JanuaryÌý2011. The Frost Group members include a trust controlled by Dr.ÌýFrost, who is the CompanyÂ’s Chief Executive Officer and Chairman of the board of directors, Dr.ÌýJane H. Hsiao, who is the Vice Chairman of the board of directors and Chief Technical Officer, Steven D. Rubin who is Executive Vice President — Administration and a director of the Company and Rao Uppaluri who is the Chief Financial Officer of the Company.
ÌýÌýÌýÌýÌýIncome taxes. For the three months ended SeptemberÌý30, 2010, our income tax provision reflects the income tax payable in Chile, partially offset by our refundable Canadian provincial tax credit. This credit relates to research and development expenses incurred at our OTI locations. The income tax benefit for the three months ended SeptemberÌý30, 2009, reflect only the refundable Canadian provincial tax credit.
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2010 AND 2009
ÌýÌýÌýÌýÌýRevenue. Revenue for the nine months ended SeptemberÌý30, 2010, was $23.0Ìýmillion, compared to $6.1Ìýmillion for the comparable 2009 period. The increase in revenue during the first nine months of 2010 is primarily due to revenue from our СÖíÊÓƵapp Chile and Exakta-СÖíÊÓƵapp pharmaceutical businesses in Chile and Mexico. We acquired СÖíÊÓƵapp Chile in OctoberÌý2009 and Exakta-СÖíÊÓƵapp in FebruaryÌý2010. As a result, the 2009 period reflects revenue only from our instrumentation business, which increased slightly during 2010.
ÌýÌýÌýÌýÌýGross margin. Gross margin for the nine months ended SeptemberÌý30, 2010, was $7.3Ìýmillion compared to $1.8Ìýmillion for the comparable period of 2009. Gross margin for the nine months ended SeptemberÌý30, 2010, increased from the 2009 period primarily as a result of the gross margin generated by our pharmaceutical business.
ÌýÌýÌýÌýÌýSelling, general and administrative expense. Selling, general and administrative expense for the nine months ended SeptemberÌý30, 2010, was $15.9Ìýmillion compared to $9.3Ìýmillion of expense for the comparable period of 2009. The increase in selling, general and administrative expenses primarily reflects the increase in selling expenses related to our pharmaceutical business, as well as professional fees. Selling, general and administrative expenses during the first nine months of 2010 and 2009, primarily include personnel expenses, including equity-based compensation expense of $3.4Ìýmillion and $2.3 million, respectively, and professional fees.
ÌýÌýÌýÌýÌýResearch and development expense. Research and development expense during the nine months ended SeptemberÌý30, 2010 and 2009, was $5.0Ìýmillion and $11.0Ìýmillion, respectively. The decrease for the nine months ended SeptemberÌý30, 2010, primarily reflects the inclusion during the 2009 period of the cost of the Phase III clinical trial for bevasiranib until MarchÌý6, 2009, when the trial was shut down. The 2009 period includes the shutdown costs of the trial, including transitioning patients from the trial onto the standard of care therapy. The shutdown costs also include the cost of analyzing the data collected and performing statistical analysis. Partially offsetting the decrease in research and development expense was increased activity related to our rolapitant and molecular diagnostic testing development programs. The nine months ended SeptemberÌý30, 2010, includes equity-based compensation expense of $0.7Ìýmillion, compared to $1.2Ìýmillion for the 2009 period.
ÌýÌýÌýÌýÌýOther operating expenses. Other operating expenses for the nine months ended SeptemberÌý30, 2010, as compared to the nine months ended SeptemberÌý30, 2009, increased by $1.6Ìýmillion primarily as a result of the amortization of the intangible assets recorded as part of the acquisition of СÖíÊÓƵapp Chile and also include amortization of intangible assets recorded as part of the acquisitions of OTI and Exakta-СÖíÊÓƵapp. The 2009 period only includes amortization of the intangible assets acquired from OTI.
ÌýÌýÌýÌýÌýOther income and expenses, net. Other income and expense, net was $1.1Ìýmillion for the first nine months of 2010 compared to $1.4Ìýmillion for the comparable 2009 period. Other income primarily consists of interest earned on our cash and cash equivalents and other expense primarily reflects the interest incurred on our line of credit with the Frost Group. The decrease reflects the repayment on JuneÌý2, 2010 of all amounts outstanding on the Frost Group line of credit.

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ÌýÌýÌýÌýÌýIncome taxes. For the nine months ended SeptemberÌý30, 2010, our income tax provision reflects the income tax payable in Chile, partially offset by our refundable Canadian provincial tax credit. This credit relates to research and development expenses incurred at our OTI locations. The income tax benefit for the nine months ended SeptemberÌý30, 2009, reflect only the refundable Canadian provincial tax credit.
LIQUIDITY AND CAPITAL RESOURCES
ÌýÌýÌýÌýÌýAt SeptemberÌý30, 2010, we had cash and cash equivalents of approximately $15.2Ìýmillion. Cash used in operations during 2010 primarily reflects expenses related to selling, general and administrative activities related to our corporate and instrumentation operations, as well as our Chilean operations. Since our inception, we have not generated sufficient income and our primary source of cash has been from the private placement of stock and through credit facilities available to us.
ÌýÌýÌýÌýÌýIn connection with our acquisition of СÖíÊÓƵapp Chile, we have outstanding lines of credit in the aggregate amount of $18.4Ìýmillion with seven financial institutions in Chile, of which, $9.8 million is unused. The average interest rate on these lines of credit is approximately 4%. These lines of credit are short-term and are generally due within three months. These lines of credit are used primarily as a source of working capital for inventory purchases. The highest balance at any time during the three months ended SeptemberÌý30, 2010 was $14.6Ìýmillion. We intend to continue to enter into these lines of credit as needed. There is no assurance that this or other funding sources will be available to us on acceptable terms, or at all.
ÌýÌýÌýÌýÌýWe currently have an unutilized $12.0Ìýmillion line of credit with the Frost Group, a related party. On JuneÌý2, 2010, we repaid all amounts outstanding on the line of credit including $12 million in principal and $4.1Ìýmillion in interest. We are obligated to pay interest upon maturity, capitalized quarterly, on outstanding borrowings under the line of credit at an 11% annual rate, which is due JanuaryÌý11, 2011. The line of credit is collateralized by all of our US based personal property except our intellectual property.
ÌýÌýÌýÌýÌýWe expect to incur losses from operations for the foreseeable future. We expect to incur substantial research and development expenses, including expenses related to the hiring of personnel and additional clinical trials. We expect that selling, general and administrative expenses will also increase as we expand our sales, marketing and administrative staff and add infrastructure.
ÌýÌýÌýÌýÌýWe believe the cash and cash equivalents on hand and available to us at SeptemberÌý30, 2010 will be sufficient to meet our anticipated cash requirements for operations and debt service for the next 12Ìýmonths. We based this estimate on assumptions that may prove to be wrong or are subject to change, and we may be required to use our available cash resources sooner than we currently expect. If we acquire additional products or companies, accelerate our product development programs or initiate additional clinical trials, we will need additional funds. Our future cash requirements will depend on a number of factors, including possible acquisitions, the continued progress of our research and development of product candidates, the timing and outcome of clinical trials and regulatory approvals, the costs involved in preparing, filing, prosecuting, maintaining, defending and enforcing patent claims, and other intellectual property rights, the status of competitive products, the availability of financing and our success in developing markets for our product candidates. If we are not able to secure additional funding when needed, we may have to delay, reduce the scope of, or eliminate one or more of our clinical trials or research and development programs.
ÌýÌýÌýÌýÌýWe intend to finance additional research and development projects, clinical trials and our future operations with a combination of private placements, payments from potential strategic research and development, licensing and/or marketing arrangements, public offerings, debt financing and revenues from future product sales, if any. There can be no assurance, however, that additional capital will be available to us on acceptable terms, or at all.
CRITICAL ACCOUNTING POLICIES AND ESTIMATES
ÌýÌýÌýÌýÌýAccounting Estimates. The preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of sales and expenses during the reporting period. Actual results could differ from those estimates.
ÌýÌýÌýÌýÌýEquity-based compensation. We recognize equity based compensation as an expense in our financial statements and that cost is measured at the fair value of the award and expensed over the vesting period. Equity-based compensation arrangements to non-employees are recorded at their fair value on the measurement date. We estimate the grant-date fair value of our stock option grants using a valuation model known as the Black-Scholes-Merton formula or the “Black-Scholes Model” and allocate the resulting compensation expense over the corresponding requisite service period associated with each grant. The Black-Scholes Model requires the use of

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several variables to estimate the grant-date fair value of stock options including expected term, expected volatility, expected dividends and risk-free interest rate. We perform significant analyses to calculate and select the appropriate variable assumptions used in the Black-Scholes Model. We also perform significant analyses to estimate forfeitures of equity-based awards. We are required to adjust our forfeiture estimates on at least an annual basis based on the number of share-based awards that ultimately vest. The selection of assumptions and estimated forfeiture rates is subject to significant judgment and future changes to our assumptions and estimates may have a material impact on our Consolidated Financial Statements.
ÌýÌýÌýÌýÌýGoodwill and intangible assets. The allocation of the purchase price for acquisitions requires extensive use of accounting estimates and judgments to allocate the purchase price to the identifiable tangible and intangible assets acquired, including in-process research and development and liabilities assumed based on their respective fair values. Additionally, we must determine whether an acquired entity is considered to be a business or a set of net assets, because a portion of the purchase price can only be allocated to goodwill in a business combination.
ÌýÌýÌýÌýÌýAppraisals inherently require significant estimates and assumptions, including but not limited to, determining the timing and estimated costs to complete the in-process research and development projects, projecting regulatory approvals, estimating future cash flows and developing appropriate discount rates. We believe the estimated fair values assigned to the Exakta-СÖíÊÓƵapp assets acquired and liabilities assumed are based on reasonable assumptions. However, the fair value estimates for the purchase price allocation may change during the allowable allocation period, which is up to one year from the acquisition date, if additional information becomes available that would require changes to our estimates.
ÌýÌýÌýÌýÌýAllowance for doubtful accounts and revenue recognition. Generally, we recognize revenue from product sales when goods are shipped and title and risk of loss transfer to our customers. Certain of our products are sold directly to end-users and require that we deliver, install and train the staff at the end-usersÂ’ facility. As a result, we do not recognize revenue until the product is delivered, installed and training has occurred. Return policies in certain international markets for our medical device products provide for stringent guidelines in accordance with the terms of contractual agreements with customers. Our estimates for sales returns are based upon the historical patterns of products returned matched against the sales from which they originated, and managementÂ’s evaluation of specific factors that may increase the risk of product returns. We analyze accounts receivable and historical bad debt levels, customer credit worthiness and current economic trends when evaluating the adequacy of the allowance for doubtful accounts using the specific identification method. Our reported net loss is directly affected by managementÂ’s estimate of the collectability of accounts receivable. The allowance for doubtful accounts recognized in our consolidated balance sheets at SeptemberÌý30, 2010 and DecemberÌý31, 2009 was $1.1 million and $0.4Ìýmillion, respectively.
ÌýÌýÌýÌýÌýRecent accounting pronouncements: In MarchÌý2010, the Financial Accounting Standards Board, or FASB, issued updated guidance to amend and clarify how entities should evaluate credit derivatives embedded in beneficial interests in securitized financial assets. The updated guidance eliminates the scope exception for bifurcation of embedded credit derivatives in interests in securitized financial assets, unless they are created solely by subordination of one financial instrument to another. The update allows entities to elect the fair value option for any beneficial interest in securitized financial assets upon adoption. This guidance is effective by the first day of the first fiscal quarter beginning after JuneÌý15, 2010. Early adoption is permitted. We have not adopted this guidance early and are currently evaluating the potential effect of the adoption of this amendment on our results of operation and financial condition.
ÌýÌýÌýÌýÌýIn MarchÌý2010, the FASB reached a consensus to issue an amendment to the accounting for revenue arrangements under which a vendor satisfies its performance obligations to a customer over a period of time, when the deliverable or unit of accounting is not within the scope of other authoritative literature, and when the arrangement consideration is contingent upon the achievement of a milestone. The amendment defines a milestone and clarifies whether an entity may recognize consideration earned from the achievement of a milestone in the period in which the milestone is achieved. This amendment is effective for fiscal years beginning on or after JuneÌý15, 2010, with early adoption permitted. The amendment may be applied retrospectively to all arrangements or prospectively for milestones achieved after the effective date. We have not adopted this guidance early and adoption of this amendment is not expected to have a material impact on our results of operation or financial condition.
ÌýÌýÌýÌýÌýIn JanuaryÌý2010, the FASB issued an amendment to the accounting for fair value measurements and disclosures. This amendment details additional disclosures on fair value measurements, requires a gross presentation of activities within a Level 3 rollforward, and adds a new requirement to the disclosure of transfers in and out of Level 1 and

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Level 2 measurements. The new disclosures are required of all entities that are required to provide disclosures about recurring and nonrecurring fair value measurements. This amendment was effective as of JanuaryÌý1, 2010, with an exception for the gross presentation of Level 3 rollforward information, which is required for annual reporting periods beginning after DecemberÌý15, 2010, and for interim reporting periods within those years. The adoption of the remaining provisions of this amendment is not expected to have a material impact on our financial statement disclosures.
ÌýÌýÌýÌýÌýIn OctoberÌý2009, the FASB issued an amendment to the accounting for multiple-deliverable revenue arrangements. This amendment provides guidance on determining whether multiple deliverables exist, how the arrangements should be separated and how the consideration paid should be allocated. As a result of this amendment, entities may be able to separate multiple-deliverable arrangements in more circumstances than under existing accounting guidance. This guidance amends the requirement to establish the fair value of undelivered products and services based on objective evidence and instead provides for separate revenue recognition based upon managementÂ’s best estimate of the selling price for an undelivered item when there is no other means to determine the fair value of that undelivered item. The existing guidance previously required that the fair value of the undelivered item reflect the price of the item either sold in a separate transaction between unrelated third parties or the price charged for each item when the item is sold separately by the vendor. If the fair value of all of the elements in the arrangement was not determinable, then revenue was deferred until all of the items were delivered or fair value was determined. This amendment will be effective prospectively for revenue arrangements entered into or materially modified in fiscal years beginning on or after JuneÌý15, 2010. Early adoption and retrospective application is also permitted. We have not adopted this guidance early and are currently evaluating the potential effect of the adoption of this amendment on our results of operations and financial condition.
ItemÌý3. Quantitative and Qualitative Disclosures About Market Risk
ÌýÌýÌýÌýÌýIn the normal course of doing business, we are exposed to the risks associated with foreign currency exchange rates and changes in interest rates.
ÌýÌýÌýÌýÌýForeign Currency Exchange Rate Risk – Our primary foreign currency exchange rate risk is derived primarily by our operations in Chile and Mexico. Although we do not speculate in the foreign exchange market, we may from time to time manage exposures that arise in the normal course of business related to fluctuations in foreign currency exchange rates by entering into offsetting positions through the use of foreign exchange forward contracts. Certain firmly committed transactions are hedged with foreign exchange forward contracts. As exchange rates change, gains and losses on the exposed transactions are partially offset by losses and gains related to the hedging contracts. Both the exposed transactions and the hedging contracts are translated at current spot rates, with gains and losses included in earnings.
ÌýÌýÌýÌýÌýOur derivative activities, which consist of foreign exchange forward contracts, are initiated to hedge forecasted cash flows that are exposed to foreign currency risk. The foreign exchange forward contracts generally require us to exchange local currencies for foreign currencies based on pre-established exchange rates at the contractsÂ’ maturity dates. As exchange rates change, gains and losses on these contracts are generated based on the change in the exchange rates that are recognized in the consolidated statement of operations at maturity, and offset the impact of the change in exchange rates on the foreign currency cash flows that are hedged. If the counterparties to the exchange contracts do not fulfill their obligations to deliver the contracted currencies, we could be at risk for currency related fluctuations. We enter into these contracts with counterparties that we believe to be creditworthy and do not enter into any leveraged derivative transactions. We had $8.0Ìýmillion in foreign exchange forward contracts outstanding at September 30, 2010, primarily to hedge Chilean-based operating cash flows against US dollars. If Chilean Pesos were to strengthen in relation to the US dollar, our hedged foreign currency cash-flows expense would be offset by a loss on the derivative contracts, with a net effect of zero.
ÌýÌýÌýÌýÌýWe do not engage in trading market risk sensitive instruments or purchasing hedging instruments or “other than trading” instruments that are likely to expose us to significant market risk, whether interest rate, foreign currency exchange, commodity price or equity price risk.
ÌýÌýÌýÌýÌýInterest Rate Risk – Our exposure to market risk relates to our cash and investments and to our borrowings. We maintain an investment portfolio of money market funds and treasury securities. The securities in our investment portfolio are not leveraged, and are, due to their very short-term nature, subject to minimal interest rate risk. We currently do not hedge interest rate exposure. Because of the short-term maturities of our investments, we do not believe that a change in market interest rates would have a significant negative impact on the value of our investment portfolio except for reduced income in a low interest rate environment. At SeptemberÌý30, 2010, we had

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cash and cash equivalents of $15.2Ìýmillion. The weighted average interest rate related to our cash and cash equivalents for the three months ended SeptemberÌý30, 2010 was 0%. As of SeptemberÌý30, 2010, the principal value of our credit lines was $8.6Ìýmillion, and have a weighted average interest rate of 5% for the nine months then ended.
ÌýÌýÌýÌýÌýThe primary objective of our investment activities is to preserve principal while at the same time maximizing yields without significantly increasing risk. To achieve this objective, we invest our excess cash in debt instruments of the U.S. Government and its agencies, bank obligations, repurchase agreements and high-quality corporate issuers and money market funds that invest in such debt instruments, and, by policy, restrict our exposure to any single corporate issuer by imposing concentration limits. To minimize the exposure due to adverse shifts in interest rates, we maintain investments at an average maturity of generally less than one month.
ItemÌý4. Controls and Procedures
ÌýÌýÌýÌýÌýThe CompanyÂ’s management, under the supervision and with the participation of the CompanyÂ’s Chief Executive Officer (“CEO”) and Chief Financial Officer (“CFO”), has evaluated the effectiveness of the CompanyÂ’s disclosure controls and procedures as defined in Securities and Exchange Commission (“SEC”) RuleÌý13a-15(e) as of SeptemberÌý30, 2010. Based on that evaluation, management has concluded that the CompanyÂ’s disclosure controls and procedures are effective to ensure that information the Company is required to disclose in reports that it files or submits under the Securities Exchange Act is accumulated and communicated to management, including the CEO and CFO, as appropriate, to allow timely decisions regarding required disclosure and is recorded, processed, summarized and reported within the time periods specified in the SECÂ’s rules and forms.
Changes to the CompanyÂ’s Internal Control Over Financial Reporting
ÌýÌýÌýÌýÌýAs part of the CompanyÂ’s SeptemberÌý30, 2010 close process, the Company identified that it had not properly accounted for a beneficial conversion feature on, and the classification of convertible preferred stock. As a result, the Company has implemented additional controls and procedures over financial reporting including adding additional review procedures on its complex accounting issues. In addition, in connection with our acquisitions of Exakta-СÖíÊÓƵapp and СÖíÊÓƵapp Chile, we continue to implement a new accounting system, as well as standards and procedures, upgrading and establishing controls over accounting systems and adding employees who are trained and experienced in the preparation of financial statements in accordance with U.S. GAAP to ensure that we have appropriate internal control over financial reporting at Exakta-СÖíÊÓƵapp and СÖíÊÓƵapp Chile. Other than as set forth above with respect to Exakta-СÖíÊÓƵapp and СÖíÊÓƵapp Chile, there have been no changes to the CompanyÂ’s internal control over financial reporting that occurred during the CompanyÂ’s third fiscal quarter that have materially affected, or are reasonably likely to materially affect, the CompanyÂ’s internal control over financial reporting.
PART II. OTHER INFORMATION
ItemÌý1. Legal Proceedings
ÌýÌýÌýÌýÌýWe are a party to litigation in the ordinary course of business. We do not believe that any such litigation will have a material adverse effect on our business, financial condition or results of operations.

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ItemÌý1A. Risk Factors
ÌýÌýÌýÌýÌýExcept as set forth below, there have been no material changes from the risk factors as previously disclosed in the Item 1A of the Company Annual Report on Form 10-K for the year ended DecemberÌý31, 2009.
ÌýÌýÌýÌýÌýThe conversion of shares of our preferred stock or exercise of warrants we have issued may result in dilution to the holders of our common stock and cause the price of our common stock to decline.
ÌýÌýÌýÌýÌýAs of SeptemberÌý30, 2010, we had 955,029 outstanding shares of SeriesÌýA Preferred Stock and 1,209,677 shares of SeriesÌýD Preferred Stock, which were convertible as of such date into 955,059 and 12,096,770 shares of our common stock, respectively, plus any accrued and unpaid dividends, if any. In addition, as of SeptemberÌý30, 2010, we had outstanding warrants to purchase 29,194,867 shares of our common stock. The conversion of outstanding shares of our SeriesÌýA Preferred Stock and SeriesÌýD Preferred Stock and the exercise of warrants may result in substantial dilution to our existing stockholders and could have a material adverse effect on our stock price. The possibility of the issuance of shares of our common stock upon the conversion of our preferred stock or the exercise of warrants could cause our stock price to decline as well. In addition, our preferred stockholders have dividend priority and liquidation preferences over shares of our common stock. Thus, the rights of the holders of common stock are and will be subject to, and may be adversely affected by, the rights of the holders of our preferred stock. As of SeptemberÌý30, 2010, our SeriesÌýA Preferred Stock and SeriesÌýD Preferred Stock had liquidation preferences of $2.6Ìýmillion and $32.4Ìýmillion, respectively.
ItemÌý2. Unregistered Sales of Equity Securities and Use of Proceeds
ÌýÌýÌýÌýÌýNone.
ItemÌý3. Defaults Upon Senior Securities
ÌýÌýÌýÌýÌýNone.
ItemÌý4. (Removed and Reserved)
ItemÌý5. Other Information
ÌýÌýÌýÌýÌýNone.
ItemÌý6. Exhibits.
Ìý Ìý Ìý
ExhibitÌý2.1(1)
Ìý Merger Agreement and Plan of Reorganization, dated as of MarchÌý27, 2007, by and among Acuity Pharmaceuticals, Inc., Froptix Corporation, eXegenics, Inc., e-Acquisition Company I-A, LLC, and e-Acquisition Company II-B, LLC.
Ìý
Ìý Ìý
ExhibitÌý2.2(4)+
Ìý Securities Purchase Agreement dated MayÌý2, 2008, among Vidus Ocular, Inc., СÖíÊÓƵapp Instrumentation, LLC, СÖíÊÓƵapp Health, Inc., and the individual sellers and noteholders named therein.
Ìý
Ìý Ìý
ExhibitÌý2.3(5)
Ìý Purchase Agreement, dated FebruaryÌý17, 2010, among Ignacio Levy García and José de Jesús Levy García, Inmobiliaria Chapalita, S.A. de C.V., Pharmacos Exakta, S.A. de C.V., СÖíÊÓƵapp Health, Inc., СÖíÊÓƵapp Health Mexicana S. de R.L. de C.V., and СÖíÊÓƵapp Manufacturing Facilities S. de R.L. de C.V.
Ìý
Ìý Ìý
ExhibitÌý3.1(2)
Ìý Amended and Restated Certificate of Incorporation.
Ìý
Ìý Ìý
ExhibitÌý3.2(3)
Ìý Amended and Restated By-Laws.
Ìý
Ìý Ìý
ExhibitÌý4.1(1)
Ìý Form of Common Stock Warrant.
Ìý
Ìý Ìý
ExhibitÌý31.1
Ìý Certification by Phillip Frost, Chief Executive Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.

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Ìý Ìý Ìý
ExhibitÌý31.2
Ìý Certification by Rao Uppaluri, Chief Financial Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
Ìý Ìý
ExhibitÌý32.1
Ìý Certification by Phillip Frost, Chief Executive Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
Ìý Ìý
ExhibitÌý32.2
Ìý Certification by Rao Uppaluri, Chief Financial Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
+ Ìý Certain confidential material contained in the document has been omitted and filed separately with the Securities and Exchange Commission.
Ìý
(1) Ìý Filed with the CompanyÂ’s Current Report on Form 8-K filed with the Securities and Exchange Commission on AprilÌý2, 2007, and incorporated herein by reference.
Ìý
(2) Ìý Filed with the CompanyÂ’s Current Report on Form 8-A filed with the Securities and Exchange Commission on JuneÌý11, 2007, and incorporated herein by reference.
Ìý
(3) Ìý Filed with the CompanyÂ’s Annual Report on Form 10-K filed with the Securities and Exchange Commission on MarchÌý31, 2008 and incorporated herein by reference.
Ìý
(4) Ìý Filed with the CompanyÂ’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on AugustÌý8, 2008 for the CompanyÂ’s three-month period ended JuneÌý30, 2008, and incorporated herein by reference.
Ìý
(5) Ìý Filed with the CompanyÂ’s Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on MayÌý10, 2010 for the CompanyÂ’s three-month period ended MarchÌý31, 2010, and incorporated herein by reference.

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SIGNATURES
ÌýÌýÌýÌýÌýPursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
Ìý Ìý Ìý Ìý Ìý
Date: November 9, 2010 Ìý СÖíÊÓƵapp Health, Inc.
Ìý
Ìý
Ìý /s/ Adam Logal Ìý Ìý
Ìý Adam LogalÌý Ìý
Ìý Executive Director of Finance,
Chief Accounting Officer and TreasurerÌý
Ìý

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ExhibitÌýIndex
Ìý Ìý Ìý
Exhibit Number Ìý Description
ExhibitÌý31.1
Ìý Certification by Phillip Frost, Chief Executive Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
Ìý Ìý
ExhibitÌý31.2
Ìý Certification by Rao Uppaluri, Chief Financial Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
Ìý Ìý
ExhibitÌý32.1
Ìý Certification by Phillip Frost, Chief Executive Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.
Ìý
Ìý Ìý
ExhibitÌý32.2
Ìý Certification by Rao Uppaluri, Chief Financial Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended SeptemberÌý30, 2010.

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