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Genadyne Biotechnologies, Inc.
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GENADYNE A4-XLR8 WOUND VACUUM SYSTEM is an FDA 510(k)-cleared medical device (K090638) manufactured by Genadyne Biotechnologies, Inc.. 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 April 28, 2009. Regulation: 8.