Endocare, Inc. - FDA 510(k) Cleared Devices

Endocare, Inc. has 22 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 22 cleared submissions from 1996 to 2010. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Endocare, Inc. Filter by specialty or product code using the sidebar.