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 Martin Medical with 14 510(k) clearances. The most recent is a 510(k) clearance dated Dec 10, 1987: PLASTER VACUUM, 230V MODEL NO. 4183-161.
| Dec 10, 1987 | PLASTER VACUUM, 230V MODEL NO. 4183-161K873723 · LGH | 510(k) clearances |
| Dec 7, 1987 | PLASTER VACUUM, 115V MODEL NO. 4183-160K873721 · LGH | 510(k) clearances |
| Oct 2, 1987 | CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135K873717 · LGF | 510(k) clearances |
| Oct 2, 1987 | CAST CUTTER, 230V MODEL NO. 4183-107K873720 · LGH | 510(k) clearances |
| Oct 2, 1987 | PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873722 · LGF | 510(k) clearances |
| Oct 2, 1987 | ADULT WALKING HEEL PRODUCT NO. 4183-130K873716 · LDF | 510(k) clearances |
| Oct 2, 1987 | CHILD WALKING HEEL PRODUCT NO. 4183-132K873718 · LGF | 510(k) clearances |
| Oct 2, 1987 | CAST CUTTER, 115V MODEL NO. 4183-106K873719 · LGH | 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
