
Porex Surgical, Inc.
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MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT is an FDA 510(k)-cleared medical device (K021357) manufactured by Porex Surgical, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 2002. Regulation: 8.