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 15, 2026, FDA's public records list Invotec International, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 2013: INVOTEC LARYNGEAL ELECTRODE.
| Oct 31, 2013 | INVOTEC LARYNGEAL ELECTRODEK122040 · ETN | 510(k) clearances |
| Dec 31, 2008 | CLEARVIEW ENDOSCOPE COVERK080740 · EOB | 510(k) clearances |
| Mar 3, 2003 | TITANIUM OSSICULAR REPLACMENT SYSTEMK030492 · ETA | 510(k) clearances |
| Dec 10, 1997 | INVOTEC CLEAN PADK973580 · EFQ | 510(k) clearances |
| Nov 6, 1997 | INVOTEC EAR TAMPON (WICK) W/STRINGK973578 · KCN | 510(k) clearances |
| May 14, 1997 | EPISTAXIS NASAL PACKK971000 · EMX | 510(k) clearances |
| Mar 19, 1993 | TRACHEOSTOMY T-TUBEK930114 · BTR | 510(k) clearances |
| Jun 4, 1991 | INVOTEC X-RAY CASSETTE EQUIPMENT DRAPEK911041 · IXA | 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
