Caiman Seal and Cut Technology

K151858 is the FDA 510(k) clearance record for Caiman Seal and Cut Technology, a class II device, cleared for Aesculap, Inc. on 2015-07-21 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 269 510(k) clearances for Aesculap, Inc., from 1991-02-06 to 2025-05-13. As of 2026-09-10, FDA records show one recall naming K151858.