Bovie J-Plasma Precise FLEX Handpiece

Bovie J-Plasma Precise FLEX Handpiece is an FDA 510(k)-cleared medical device (K170777) manufactured by 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 April 30, 2017. Regulation: 8.