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Uroplasty, Inc.

8 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
UROPLASTY RIGID ENDOSCPIC NEEDLES (K121337)Uroplasty, Inc.2012-08-03
URGENT PC STIMULATOR; URGENT PC LEAD SET (K101847)Uroplasty, Inc.2010-10-21
UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518 (K091391)Uroplasty, Inc.2009-06-30
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12 (K071822)Uroplasty, Inc.2007-08-20
URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12 (K061333)Uroplasty, Inc.2006-07-03
URGENT PC NEUROMODULATION SYSTEM (K052025)Uroplasty, Inc.2005-10-17
I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000 (K052175)Uroplasty, Inc.2005-10-17
UROPLASTY RIGID ENDOSCOPIC NEEDLE (K051905)Uroplasty, Inc.2005-08-29

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Every clearance here is in the API, with alerts when new ones post.