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 Innervision with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 10, 1999: CHRISTOUDIAS SLIM TIP ELECTRODE INSERT.
| Date | Record | Source |
|---|---|---|
| Sep 10, 1999 | CHRISTOUDIAS SLIM TIP ELECTRODE INSERTK992345 · GEI | 510(k) clearances |
| Aug 6, 1999 | MACMED PAEDIATRIC INTRAMEDULLARY NAILK991877 · JDS | 510(k) clearances |
| Oct 9, 1998 | CHRISTOUDIAS GAUZE DISSECTOR (LAPAROSCOPIC HAND INSTRUMENT)K982428 · HET | 510(k) clearances |
| Sep 13, 1994 | INNERVISION INC. CANNULA/TROCAR,MULTIPLE TYPESK940731 · GCJ | 510(k) clearances |
| Aug 23, 1994 | INNERVISION,INC. LAPAROSCOPIC ELECTRODESK940750 · GEI | 510(k) clearances |
| Jul 22, 1994 | INNERVISION INC. LAPAROSCOPIC HAND INSTRUMENTSK940718 · HET | 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
