
Ceremed , Inc.
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Biopor, AOC Porous Polyethylene, Cerepor is an FDA 510(k)-cleared medical device (K160988) manufactured by Ceremed , Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 2016. Regulation: 8.