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Stryker Leibinger GmbH & Co KG
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STRYKER BIPOLAR FORCEPS is an FDA 510(k)-cleared medical device (K093108) manufactured by Stryker Leibinger GmbH & Co KG. 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 June 21, 2010. Regulation: 8.