Renuvion APR Handpiece

Renuvion APR Handpiece is an FDA 510(k)-cleared medical device (K220970) 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 July 14, 2022. Regulation: 8.