
Cynosure, Inc.
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CYNOSURE PHOTOTOME SURGICAL DIODE LASER is an FDA 510(k)-cleared medical device (K935305) manufactured by Cynosure, 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 March 17, 1994. Regulation: 8.