Inno-Port Disposable Bladed Trocar

K252532 is the FDA 510(k) clearance record for Inno-Port Disposable Bladed Trocar, a class II device, cleared for Taiwan Surgical Corporation on 2026-06-02 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 8 510(k) clearances for Taiwan Surgical Corporation, from 2015-04-01 to 2026-07-20. As of 2026-09-10, FDA records show no recalls naming K252532.