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 Ace Orthopedic Manufacturing Co. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Mar 22, 1994: AIM SUPRACONDYLAR NAIL.
| Mar 22, 1994 | AIM SUPRACONDYLAR NAILK934962 · HSB | 510(k) clearances |
| Mar 22, 1994 | ACE HUMERAL NAILK934643 · HSB | 510(k) clearances |
| Feb 22, 1994 | ACE UNILATERAL FIXATOR IIK936045 · JEC | 510(k) clearances |
| Mar 31, 1993 | ACE 8.0MM CANNULATED CANCELLOUS BONE SCREWK926047 · HWC | 510(k) clearances |
| Jul 27, 1992 | ACE 100 DEGREES TUBULAR PLATEK920738 · HRS | 510(k) clearances |
| Jan 12, 1982 | ACE/KYLE CAPTURED HIP SCREWK813554 · KTT | 510(k) clearances |
| Mar 20, 1981 | TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONGK810193 · HAX | 510(k) clearances |
| Sep 9, 1980 | ACE FISCHER EXTERNAL FIXATION DEVICEK801594 · HXK | 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
