Bovie Medical Corporation - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Bovie Medical Corporation has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Clearwater, US.
Historical record: 14 cleared submissions from 2009 to 2019.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bovie Medical Corporation
14 devices
Cleared
Mar 12, 2019
Renuvion/J-Plasma Precise Handpiece, Renuvion/J-Plasma Precise Open...
General & Plastic Surgery
76d
Cleared
May 01, 2017
Bovie J-Plasma Precise FLEX Handpiece
General & Plastic Surgery
47d
Cleared
Mar 08, 2017
Bovie J-Plasma Precise Open handpiece & Bovie Ultimate Gen 2 High Frequency...
General & Plastic Surgery
44d
Cleared
Jul 29, 2016
Bovie 3.3mm Disposable Bipolar Ablator 90°, Aspirating and Non-Aspirating,...
General & Plastic Surgery
53d
Cleared
Jun 20, 2016
Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical...
General & Plastic Surgery
59d
Cleared
Jan 15, 2016
Bovie Disposable Bipolar Ablator
General & Plastic Surgery
112d
Cleared
Nov 02, 2015
Bovie J-Plasma Precise 360 Handpiece
General & Plastic Surgery
54d
Cleared
Aug 04, 2015
Bovie J-Plasma Handpiece
General & Plastic Surgery
78d
Cleared
Dec 12, 2014
Bovie Ultimate High Frequency Electrosurgical Generator
General & Plastic Surgery
59d
Cleared
Mar 17, 2014
BOVIE IDS-310 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A3350 HIGH...
General & Plastic Surgery
76d
Cleared
Jul 20, 2012
CAUTERY
Ophthalmic
66d
Cleared
Jan 27, 2012
BOVIE J-PLASMA HANDPIECE WITH RETRACTABLE CUTTING BLADE
General & Plastic Surgery
176d