Remanufactured EndoWrist Cobra Grasper (420190)

Remanufactured EndoWrist Cobra Grasper (420190) is an FDA 510(k)-cleared medical device (K250417) 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 19, 2025. Regulation: 8.