Bovie Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bovie Medical - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Bovie Medical has 8 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.
Historical record: 8 cleared submissions from 2006 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bovie Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bovie Medical
8 devices
Cleared
Mar 18, 2010
BOSS COAGULATION DEVICE, MODEL BOSS1215, BOSS COAGULATION DEVICE, ANGLED...
General & Plastic Surgery
245d
Cleared
Oct 09, 2009
LAPAROSCOPIC RESECTION DEVICE, MODEL SR326L
General & Plastic Surgery
147d
Cleared
Aug 07, 2009
BOVIE ICON GS ELECTROSURGICAL GENERATOR (GS100), HANDPIECE (GS-OP-R),...
General & Plastic Surgery
156d
Cleared
Nov 17, 2008
SALINE ENHANCED ELECTROSURGICAL RESECTION (SEER) DEVICE
General & Plastic Surgery
74d
Cleared
Oct 02, 2008
BOVIE ICON GENERAL PURPOSE RF GENERATOR
General & Plastic Surgery
69d
Cleared
Jul 24, 2008
MEG LAPAROSCOPIC ELECTRODES
General & Plastic Surgery
64d
Cleared
Apr 10, 2008
BOVIE IDS-400 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
260d
Cleared
Sep 06, 2006
BOVIE ICON GI ELECTROSURGICAL GENERATOR, MODEL GI 120
General & Plastic Surgery
65d