Remanufactured EndoWrist Long Tip Forceps (420048)

Remanufactured EndoWrist Long Tip Forceps (420048) is an FDA 510(k)-cleared medical device (K250387) manufactured by Rebotix. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 2025. Regulation: 8.