Uroplasty, Inc. is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Uroplasty, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UROPLASTY RIGID ENDOSCPIC NEEDLES, URGENT PC STIMULATOR, UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518
8
Total
8
Cleared
0
Denied
Uroplasty, Inc. has 8 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 8 cleared submissions from 2005 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Uroplasty, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Uroplasty, Inc.
8 devices
Cleared
Aug 03, 2012
UROPLASTY RIGID ENDOSCPIC NEEDLES
Gastroenterology & Urology
92d
Cleared
Oct 21, 2010
URGENT PC STIMULATOR
Gastroenterology & Urology
112d
Cleared
Jun 30, 2009
UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518
Gastroenterology & Urology
50d
Cleared
Aug 20, 2007
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12
Gastroenterology & Urology
48d
Cleared
Jul 03, 2006
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12
Gastroenterology & Urology
52d
Cleared
Oct 17, 2005
URGENT PC NEUROMODULATION SYSTEM
Gastroenterology & Urology
82d
Cleared
Oct 17, 2005
I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000
Gastroenterology & Urology
68d
Cleared
Aug 29, 2005
UROPLASTY RIGID ENDOSCOPIC NEEDLE
Gastroenterology & Urology
46d