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CPC Files Patent for Synthetic Sealant for the MedClose(TM) Vascular Closure System (VCS)
Date:5/21/2009

anding issues with the FDA concerning our application for an investigational device exemption.

We believe that our sealant offers some important advantages over the plasma-based sealant we had intended to utilize in several respects. As a synthetic sealant, our product is free from the risk of blood-borne and other pathogens. Also, testing to date indicates that our sealant is highly adhesive and may ultimately prove to be more adhesive than any other plasma-based sealant presently available. In addition, these tests show that our sealant has excellent adhesive strengths when applied to wet areas and may have greater adhesive strength on wet areas than any other sealant on the market, which could be a tremendous competitive advantage due to the fact that vascular closure sites are normally initially wet due to arterial bleeding from the arteriotomy. Finally, the synthetic sealant appears to perform independently with respect to the level of anti-coagulation present.

About CPC

CPC of America develops therapeutic devices for use in endovascular procedures. CPC's current focus is the completion of development and testing of the MedClose(TM) 6-9Fr vascular closure system, an internal puncture-closing system for use in catheter laboratories and interventional radiological procedures. CPC is also focusing on its own synthetic sealant product line for various applications and not just limited to vascular closure applications of various sizes.

Forward Looking Statements

The statements contained in this press release that are not historical are "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended (the "Securities Act"), and Section 21E of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), including statements, without limitation, regarding the Company's expectations, beliefs, intentions or strategies rega
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SOURCE CPC of America, Inc.
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