ClearanceBrief
Company ยท US

Uroplasty, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2012. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NAMStimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence4
FBKEndoscopic Injection Needle, Gastroenterology-Urology3
OTNMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 3, 2012K121337UROPLASTY RIGID ENDOSCPIC NEEDLES
Uroplasty, Inc.
FBK
Oct 21, 2010K101847URGENT PC STIMULATOR; URGENT PC LEAD SET
Uroplasty, Inc.
NAM
Jun 30, 2009K091391UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518
Uroplasty, Inc.
FBK
Aug 20, 2007K071822URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12
Uroplasty, Inc.
NAM
Jul 3, 2006K061333URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12
Uroplasty, Inc.
NAM
Oct 17, 2005K052175I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000
Uroplasty, Inc.
OTN
Oct 17, 2005K052025URGENT PC NEUROMODULATION SYSTEM
Uroplasty, Inc.
NAM
Aug 29, 2005K051905UROPLASTY RIGID ENDOSCOPIC NEEDLE
Uroplasty, Inc.
FBK

Latest recalls

DateFirm and productCodeLinked 510(k)
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