Renuvion Dermal Handpiece, Renuvion Dermal System

Renuvion Dermal Handpiece, Renuvion Dermal System is an FDA 510(k)-cleared medical device (K211652) manufactured by Apyx Medical Corporation (Formerly Bovie Medical Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 24, 2022. Regulation: 8.