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 Acuderm with 13 510(k) clearances. The most recent is a 510(k) clearance dated Mar 24, 1994: ACU-E PUNCH.
| Date | Record | Source |
|---|---|---|
| Mar 24, 1994 | ACU-E PUNCHK933516 · LRY | 510(k) clearances |
| Mar 7, 1994 | ACU-DISPO-CE(TM)K933265 · MDM | 510(k) clearances |
| Feb 22, 1994 | ACU-SUTURE KITK933137 · LRO | 510(k) clearances |
| Feb 9, 1994 | ACU-EVACK930043 · FYD | 510(k) clearances |
| Dec 1, 1993 | ACU-HEMOSTATIC RINGK933866 · MDM | 510(k) clearances |
| Jan 27, 1992 | ACU-GUARDK915000 · GEX | 510(k) clearances |
| Apr 11, 1989 | ACU-CURETTEK891334 · FZS | 510(k) clearances |
| Nov 23, 1987 | ACU-MICRO-NEEDLEK874024 · FMI | 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
