Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Acu-Med, Inc. with 48 510(k) clearances. The most recent is a 510(k) clearance dated Jul 17, 2002: WRIST FUSION PLATE.
| Jul 17, 2002 | WRIST FUSION PLATEK021321 · HRS | 510(k) clearances |
| Dec 19, 2001 | POLARUS CAP SCREWK013616 · HSB | 510(k) clearances |
| Nov 7, 2001 | CONGRUENT BONE PLATE SYSTEMK012655 · HRS | 510(k) clearances |
| Feb 4, 2000 | ACUMED MODULAR SHOULDER SYSTEMK992525 · HSD | 510(k) clearances |
| Jan 13, 2000 | ACUMED SUTURE ANCHORK993657 · MBI | 510(k) clearances |
| Mar 16, 1998 | ACUMED SUTURE ANCHORK980103 · MBI | 510(k) clearances |
| Mar 17, 1997 | ACUMED SUTURE WASHERK965028 · HTN | 510(k) clearances |
| Feb 19, 1997 | STABLELOC II EXTERNAL FIXATORK965029 · JEC | 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
