Vivant Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivant Medical, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Vivant Medical, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Portola Valley, US.
Historical record: 10 cleared submissions from 2000 to 2005.
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) Regulatory Record - Vivant Medical, Inc.
10 devices
Cleared
Feb 24, 2005
VIVAWAVE MICROWAVE ABLATION SYSTEM, COAXIAL INTRODUCER
General & Plastic Surgery
24d
Cleared
Mar 02, 2004
VIVARING MICROWAVE ABLATION PROBE
General & Plastic Surgery
26d
Cleared
Oct 03, 2003
VIVATIP MICROWAVE ABLATION PROBE
General & Plastic Surgery
31d
Cleared
Aug 06, 2003
TRI-LOOP MICROWAVE ABLATION PROBE
General & Plastic Surgery
35d
Cleared
Jun 23, 2003
VIVATHERM THEMPERATURE MEASUREMENT SYSTEM
General Hospital
35d
Cleared
Apr 09, 2003
LOOP MICROWAVE ABLATION PROBE
General & Plastic Surgery
188d
Cleared
Oct 11, 2002
ENCIRCLE LOCALIZATION DEVICE
Gastroenterology & Urology
88d
Cleared
Jun 18, 2002
VIVAWAVE MICROWAVE SYSTEM
General & Plastic Surgery
384d
Cleared
Dec 15, 2000
VIVANT BREAST LESION LOCALIZATION DEVICE
Gastroenterology & Urology
39d
Cleared
Jun 23, 2000
VIVANT MEDICAL BIOPSY MARKER SYSTEM
General & Plastic Surgery
144d