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Medica-Rents Co., Ltd.
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PROSPERA PRO-I, PRO-II AND PRO-III NEGATIVE PRESSURE WOUND THERAPY SYSTEM is an FDA 510(k)-cleared medical device (K112458) manufactured by Medica-Rents Co., Ltd.. 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 January 4, 2012. Regulation: 8.