Usgi Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Usgi Medical - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Usgi Medical has 11 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Historical record: 11 cleared submissions from 2005 to 2011. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Usgi Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Usgi Medical
11 devices
Cleared
Jan 14, 2011
G-PROX EZ ENDOSCOPIC GRASPER
Gastroenterology & Urology
28d
Cleared
Dec 30, 2010
G-CINCH SUTURE GRASPER
Gastroenterology & Urology
87d
Cleared
Oct 20, 2010
G-CATH TISSUE ANCHOR DELIVERY CATHETER
General & Plastic Surgery
19d
Cleared
Feb 17, 2010
G-CATH TISSUE ANCHOR DELIVERY CATHETER, MODELS 205302, 205333
General & Plastic Surgery
20d
Cleared
Oct 07, 2009
G-PROX ENDOSCOPIC GRASPER, MODEL 205333
General & Plastic Surgery
29d
Cleared
Sep 13, 2007
USGI TRANSPORT ENDOSCOPIC ACCESS DEVICE
Gastroenterology & Urology
17d
Cleared
Dec 06, 2006
G-PROX ENDOSCOPIC GRASPER
General & Plastic Surgery
212d
Cleared
Jul 31, 2006
G-LIX TISSUE GRASPER
Obstetrics & Gynecology
87d
Cleared
May 15, 2006
USGI TRANSPORT ENDOSCOPIC GUIDE
Gastroenterology & Urology
13d
Cleared
Jul 26, 2005
MODIFICATION TO: USGI SHAPELOCK ENDOSCOPIC GUIDE
Gastroenterology & Urology
11d
Cleared
Feb 28, 2005
USGI SHAPELOCK ENDOSCOPIC GUIDE
Gastroenterology & Urology
25d