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 14, 2026, FDA's public records list Endovations with 38 510(k) clearances. The most recent is a 510(k) clearance dated Feb 8, 1996: ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETER.
| Feb 8, 1996 | ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETERK955413 · FGE | 510(k) clearances |
| Oct 13, 1994 | INJECT-SNAREK942110 · FDI | 510(k) clearances |
| Oct 11, 1994 | OXYGEN MOUTHGUARDK944049 · MNK | 510(k) clearances |
| Feb 28, 1994 | ENDOVATIONS(R) .035 PRE-CUT PAPILLATOMEK934315 · KNS | 510(k) clearances |
| Oct 8, 1991 | 2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATHK913841 · FGE | 510(k) clearances |
| Sep 16, 1991 | 5MM MICROSCISSORSK913870 · GCJ | 510(k) clearances |
| Aug 7, 1991 | OVAL CUP BIOPSY FORCEPK911155 · FCF | 510(k) clearances |
| May 31, 1989 | ENDO-SPONGEK892218 · MNL | 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
