
Porex Technologies Corp.
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MEDPOR SURG IMPLANT MATERIAL:PREFOR CRAN/FAC IMPLA is an FDA 510(k)-cleared medical device (K922489) manufactured by Porex Technologies Corp.. 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 September 1, 1992. Regulation: 8.