Canady Flex RoboWrist

Canady Flex RoboWrist is an FDA 510(k)-cleared medical device (K212736) manufactured by Us Medical Innovations, LLC. 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 November 21, 2022. Regulation: 8.