Apple Medical Mobius Elastic Retractor

K014005 is the FDA 510(k) clearance record for APPLE MEDICAL MOBIUS ELASTIC RETRACTOR, a class II device, cleared for Apple Medical Corp. on 2002-02-15 under FDA product code GCJ (Laparoscope, General & Plastic Surgery). FDA's definition for product code GCJ 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 103 510(k) clearances for COOPERSURGICAL, INC., from 1981-02-04 to 2026-01-20. As of 2026-09-10, FDA records show no recalls naming K014005.