Vnus Medical Technologies, Inc. is one of 20536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vnus Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2, VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100, VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15)
9
Total
9
Cleared
0
Denied
Vnus Medical Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 9 cleared submissions from 1998 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vnus Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vnus Medical Technologies, Inc.
9 devices
Cleared
Oct 15, 2008
VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2
General & Plastic Surgery
15d
Cleared
Aug 01, 2006
VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100
General & Plastic Surgery
76d
Cleared
Oct 11, 2005
VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15)
General & Plastic Surgery
78d
Cleared
Jun 07, 2004
VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2
General & Plastic Surgery
89d
Cleared
Jan 07, 2004
VNUS VESSEL AND TISSUE COAGULATION SYSTEM
General & Plastic Surgery
56d
Cleared
Mar 11, 2003
MODIFICATION TO VNUS CLOSURE SYSTEM
General & Plastic Surgery
18d
Cleared
Dec 18, 2000
MODIFICATION TO VNUS CLOSURE SYSTEM
General & Plastic Surgery
76d
Cleared
Mar 17, 1999
VNUS CLOSURE SYSTEM
General & Plastic Surgery
218d
Cleared
Feb 20, 1998
VNUS CLOSURE SYSTEM
General & Plastic Surgery
80d