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Medicis Technologies Corporation
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LIPOSONIX SYSTEM, MODEL 1 P00XXXX is an FDA 510(k)-cleared medical device (K100874) manufactured by Medicis Technologies Corporation. 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 August 18, 2011. Regulation: 8.