Covidien, Formerly Valleylab, A Division of Tyco H is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien, Formerly Valleylab, A Division of Tyco H - FDA 510(k) Clear...
6
Total
6
Cleared
0
Denied
Covidien, Formerly Valleylab, A Division of Tyco H has 6 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 6 cleared submissions from 2011 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covidien, Formerly Valleylab, A Division of Tyco H Filter by specialty or product code using the sidebar.
Covidien, Formerly Valleylab, A Division of Tyco H — FDA 510(k) Products and Clearance History
6 devices
Cleared
Aug 07, 2014
SONICISION CORDLESS ULTRASONIC DISSECTOR
General & Plastic Surgery
72d
Cleared
Dec 20, 2013
LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX)
General & Plastic Surgery
51d
Cleared
Aug 28, 2013
SONICISION STERILIZATION TRAY
General Hospital
126d
Cleared
Jan 30, 2013
LIGASURE IMPACT CURVED, LARGE JAW, OPEN SEALER / DIVIDER
General & Plastic Surgery
83d
Cleared
Sep 05, 2012
LIGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER
General & Plastic Surgery
278d
Cleared
May 06, 2011
FORCETRIAD
General & Plastic Surgery
217d