Medical Device Manufacturer · US , Minneapolis , MN

Uroplasty, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005

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.

Uroplasty, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Uroplasty, Inc.

8 devices

1-8 of 8

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