Stryker Bipolar Forceps

K093108 is the FDA 510(k) clearance record for STRYKER BIPOLAR FORCEPS, a class II device, cleared for Stryker Leibinger GmbH & Co KG on 2010-06-22 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 22 510(k) clearances for Stryker Leibinger GmbH & Co KG, from 2009-02-19 to 2026-07-01. As of 2026-09-10, FDA records show no recalls naming K093108.