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CPC Pursues Development of Proprietary Synthetic Sealants as part of MedClose(TM) Global Commercialization
Date:3/10/2009

f manufacturing of the MedClose system, (2) the Company's ability to successfully develop proprietary synthetic sealants and integrate any such sealants as part of the MedClose device, (3) regulatory approvals of the MedClose system including any proprietary synthetic sealants, and (4) those other risks and factors described from time to time in the Company's reports filed with the Securities and Exchange Commission, including but not limited to the Company's Annual Report on Form 10-K for the year ended December 31, 2008 and subsequently filed Forms 10-Q and Forms 8-K. The Company cautions readers not to place undue reliance on any forward-looking statements. The Company does not undertake, and specifically disclaims any obligation, to update or revise such statements to reflect new circumstances or unanticipated events as they occur.

(1) Fibrin versus polyethylene glycol sealant: an experimental study in rabbits." European Journal of Plastic Surgery (v 31, No. 5). October, 2008


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SOURCE CPC of America, Inc.
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