Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of OlympusLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Uroplasty with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 3, 2012: UROPLASTY RIGID ENDOSCPIC NEEDLES.
| Date | Record | Source |
|---|---|---|
| Aug 3, 2012 | UROPLASTY RIGID ENDOSCPIC NEEDLESK121337 · FBK | 510(k) clearances |
| Oct 21, 2010 | URGENT PC STIMULATOR; URGENT PC LEAD SETK101847 · NAM | 510(k) clearances |
| Jun 30, 2009 | UROPLASTY RIGID ENDOSCOPIC NEEDLE, MRN-518K091391 · FBK | 510(k) clearances |
| Aug 20, 2007 | URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200 AND UPC250-12K071822 · NAM | 510(k) clearances |
| Jul 3, 2006 | URGENT PC NEUROMODULATION SYSTEM, MODELS UPC200-A AND UPC250-12K061333 · NAM | 510(k) clearances |
| Oct 17, 2005 | URGENT PC NEUROMODULATION SYSTEMK052025 · NAM | 510(k) clearances |
| Oct 17, 2005 | I-STOP MID-URETHRAL SLING, MODELS IS-1000, IS-2000, IS-3000, IS-4000K052175 · OTN | 510(k) clearances |
| Aug 29, 2005 | UROPLASTY RIGID ENDOSCOPIC NEEDLEK051905 · FBK | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
