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Somatex Medical Technologies GmbH
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TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560 is an FDA 510(k)-cleared medical device (K073095) manufactured by Somatex Medical Technologies GmbH. 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 18, 2008. Regulation: 8.