Medical device makerLabelled 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 Ovamed with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 20, 1995: HYSTEROSYS FLEXIBLE HYSTEROCOPE.
| Date | Record | Source |
|---|---|---|
| Nov 20, 1995 | HYSTEROSYS FLEXIBLE HYSTEROCOPEK951946 · HIH | 510(k) clearances |
| Jul 28, 1995 | OVAMED INTRAUTERINE ACCESS CATHETERK931534 · MOV | 510(k) clearances |
| Jun 22, 1995 | OVAMED FALLOPIAN OSTIAL ACCESS CATHETERK931167 · LKF | 510(k) clearances |
| Mar 22, 1995 | SARATOGA MODULAR MINIATURE ENDOSCOPE SYSTEMK943593 · ODF | 510(k) clearances |
| Jan 30, 1995 | OVAMED HSG CATHETERK931122 · LKF | 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
