Black and Black Electrosurgical Cutting and Coagulation Forceps and Electrodes

K072124 is the FDA 510(k) clearance record for BLACK AND BLACK ELECTROSURGICAL CUTTING AND COAGULATION FORCEPS AND ELECTRODES, a class II device, cleared for Black & Black Surgical, Inc. on 2008-01-18 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 4 510(k) clearances for Black & Black Surgical, Inc., from 2008-01-18 to 2024-09-13. As of 2026-09-10, FDA records show no recalls naming K072124.