J-Plasma Precise FLEX Handpiece

J-Plasma Precise FLEX Handpiece is an FDA 510(k)-cleared medical device (K202880) 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 January 3, 2021. Regulation: 8.