SURGILON, DERMALON, & OPHTHALON

SURGILON, DERMALON, & OPHTHALON is an FDA 510(k)-cleared medical device (K981582) manufactured by Davis & Geck, 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 12, 1998. Regulation: 8.