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Vivoxid , Ltd.
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BONALIVE GRANULES AND BONALIVE PLATES is an FDA 510(k)-cleared medical device (K071937) manufactured by Vivoxid , 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 October 18, 2007. Regulation: 8.