Valleylab is one of 21843 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Valleylab - FDA 510(k) Cleared Devices
Recent clearances: LIGASURE 5MM BLUNT TIP LAPAROSCOPIC SEALER-DIVIDER, LIGASURE ADVANCE LAPAROSCOPIC SEALER/DIVIDER WITH DISSECTING ELECTRODE, MODELS LF5034 AND LF5044, VIVAWAVE MICROWAVE ABLATION SYSTEM
10
Total
10
Cleared
0
Denied
Valleylab has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Boulder, US.
Historical record: 10 cleared submissions from 2004 to 2009.
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 - Valleylab
10 devices
Cleared
Oct 16, 2009
LIGASURE 5MM BLUNT TIP LAPAROSCOPIC SEALER-DIVIDER
General & Plastic Surgery
28d
Cleared
Nov 29, 2006
LIGASURE ADVANCE LAPAROSCOPIC SEALER/DIVIDER WITH DISSECTING ELECTRODE,...
General & Plastic Surgery
40d
Cleared
Apr 27, 2006
VIVAWAVE MICROWAVE ABLATION SYSTEM
General & Plastic Surgery
129d
Cleared
Mar 15, 2006
COOL-TIP RF GENERATOR, COOL-TIP RF SYSTEM ACCESSORIES
General & Plastic Surgery
110d
Cleared
Feb 03, 2006
COOL-TIP RF GENERATOR, COOL-TIP RF SYSTEM ACCESSORIES
General & Plastic Surgery
123d
Cleared
Aug 11, 2005
VALLEYLAB FORCETRIAD ELECTROSURGICAL GENERATOR
General & Plastic Surgery
52d
Cleared
Jul 22, 2005
VALLEYLAB G3000 ELECTROSURGICAL INSTRUMENT
General & Plastic Surgery
32d
Cleared
Jan 05, 2005
LIGASURE VESSEL SEALING SYSTEM. LIGASURE INSTRUMENTS
General & Plastic Surgery
40d
Cleared
Nov 12, 2004
COOL-TIP RF ABLATION SYSTEM
General & Plastic Surgery
88d
Cleared
Sep 28, 2004
LIGASURE PRECISE MODEL #LS1200/LIGASURE 5MM LAPAROSCOPIC SEALER DIVIDER MODEL...
General & Plastic Surgery
106d