
Surgilase, Inc.
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SURGIPROBES AND SURGISCALPES IN HEAD/NECK SURGERY is an FDA 510(k)-cleared medical device (K894471) manufactured by Surgilase, 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 November 13, 1989. Regulation: 8.