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 14, 2026, FDA's public records list Ormed Manufacturing with 23 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 1994: ARTROMOT K2 CPM.
| Jan 31, 1994 | ARTROMOT K2 CPMK931555 · BXB | 510(k) clearances |
| Jul 18, 1988 | CYLINDRICAL SPONGEK882528 · EFQ | 510(k) clearances |
| Jul 18, 1988 | GAUZE SPONGEK882527 · EFQ | 510(k) clearances |
| Jul 18, 1988 | TAPE STRUNG TONSIL SPONGEK882530 · EFQ | 510(k) clearances |
| Jul 18, 1988 | BUTCHER STRUNG TONSIL SPONGEK882529 · EFQ | 510(k) clearances |
| Mar 17, 1988 | ROSEBUD DISSECTORSK880852 · EFQ | 510(k) clearances |
| Mar 17, 1988 | ROUND STICK SPONGESK880910 · EFQ | 510(k) clearances |
| Mar 17, 1988 | TRACHEOTOMY SPONGESK880909 · EFQ | 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
