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 Omnicon Medical with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 21, 1983: EMERGENCY TRACHEOSTOMY KIT.
| Jan 21, 1983 | EMERGENCY TRACHEOSTOMY KITK823872 · EWC | 510(k) clearances |
| Mar 18, 1982 | ANESTHESIA BACTERIA FILTERK820577 · CAH | 510(k) clearances |
| Mar 18, 1982 | MAINFLOW BACTERIA FILTERK820576 · CAH | 510(k) clearances |
| Aug 13, 1980 | MAINFLOW BACTERIA FILTERK801803 · CAH | 510(k) clearances |
| Aug 13, 1980 | ANESTHESIA BACTERIA FILTERK801804 · CAH | 510(k) clearances |
| Dec 20, 1977 | PROTECT IV GARDK772060 · FMP | 510(k) clearances |
| Feb 14, 1977 | DISPOSABLE BACTERIA FILTERK770136 · CAH | 510(k) clearances |
| Jan 12, 1977 | AIRWAY, BERMAN 40, 60, 80, 90, L00MM'SK770001 · CAE | 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
