Arthrex Opes Electrodes and Accessories

K023986 is the FDA 510(k) clearance record for ARTHREX OPES ELECTRODES AND ACCESSORIES, a class II device, cleared for Arthrex, Inc. on 2002-12-17 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 352 510(k) clearances for Arthrex, Inc., from 1992-03-19 to 2026-08-07. As of 2026-09-10, FDA records show no recalls naming K023986.