Vygon Corp. - FDA 510(k) Cleared Devices
48
Total
46
Cleared
0
Denied
Vygon Corp. has 46 FDA 510(k) cleared medical devices. Based in East Rutherford, US.
Historical record: 46 cleared submissions from 1985 to 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vygon Corp. Filter by specialty or product code using the sidebar.
48 devices
Cleared
Dec 18, 2012
NUTRISAFE 2 FEEDING TUBE
Gastroenterology & Urology
250d
Cleared
Oct 13, 2011
NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXX
Gastroenterology & Urology
631d
Cleared
May 06, 2008
HEPATOSTAT SET
General & Plastic Surgery
146d
Cleared
Nov 30, 2007
MODIFICATION TO: LATEX-FREE BIONECTOR, MODEL# 896.019, 896.039
General Hospital
261d
Cleared
Nov 02, 2006
HEPATOSTAT SET, MODEL 760X
General & Plastic Surgery
129d
Cleared
Sep 29, 2006
MULTICATH EXPERT
General Hospital
148d
Cleared
Sep 15, 2006
NUTRISAFE 2
Gastroenterology & Urology
162d
Cleared
Sep 15, 2006
LIFECATH S PICC AND MIDLINE CATHETER
General Hospital
28d
Cleared
Apr 05, 2006
VYGON LEADER-FLEX
General Hospital
198d
Cleared
Mar 02, 2006
VYGON LATEX FREE BIONECTOR
General Hospital
141d
Cleared
Oct 27, 2005
VYGON MICRO-ACCESS SAFETY INTRODUCER KIT
Cardiovascular
164d
Cleared
Aug 19, 2005
VYGON NUTRILINE CATHETERS
General Hospital
57d
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