Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Mpathy Medical Devices with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 12, 2009: OMNISURE URETHRAL SLING, MODEL OTK52.
| Aug 12, 2009 | OMNISURE URETHRAL SLING, MODEL OTK52K092203 · OTN | 510(k) clearances |
| Aug 4, 2009 | RESTORELLE POLYPROPYLENE MESHK092207 · OTP | 510(k) clearances |
| Jul 14, 2009 | MINITAPE URETHRAL SLINGK091180 · PAH | 510(k) clearances |
| Mar 3, 2008 | MINITAPE EXTRA URETHRAL SLINGK073647 · OTN | 510(k) clearances |
| Feb 25, 2008 | MINITAPE URETHRAL SLINGK073646 · PAH | 510(k) clearances |
| Feb 6, 2006 | MODIFICATION TO: MINIMESH POLYPROPYLENE MESHK053361 · OTO | 510(k) clearances |
| Nov 17, 2004 | MINIMESH POLYPROPYLENE MESHK041632 · OTO | 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
