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Cynosure, Inc.
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ASA 'MPHI FAMILY DIODE LASER is an FDA 510(k)-cleared medical device (K111901) manufactured by Cynosure, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 8, 2011. Regulation: 8.