
Bovie Medical Corporation
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Bovie J-Plasma Precise Open handpiece & Bovie Ultimate Gen 2 High Frequency Electrosurgical Generator is an FDA 510(k)-cleared medical device (K170188) 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 March 7, 2017. Regulation: 8.