Non Stick Bipolar Forceps Model 07/Xxx, Bipolar Forceps Model 08/Xxx, Monopolar Forceps Model 09/Xxx

K101080 is the FDA 510(k) clearance record for NON STICK BIPOLAR FORCEPS MODEL 07/XXX, BIPOLAR FORCEPS MODEL 08/XXX, MONOPOLAR FORCEPS MODEL 09/XXX, a class II device, cleared for Egon Faulhaber Surgical Instruments Pinzetten on 2010-06-21 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 one 510(k) clearance for Egon Faulhaber Surgical Instruments Pinzetten. As of 2026-09-10, FDA records show no recalls naming K101080.