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 Cintor Orthopaedic Div. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 9, 1981: RADIAL HEAD PROSTHESIS.
| Jun 9, 1981 | RADIAL HEAD PROSTHESISK811451 · JDB | 510(k) clearances |
| Apr 7, 1981 | KNEE PROSTHESISK810540 · HRY | 510(k) clearances |
| Feb 23, 1981 | HARRIS CEMENT RESTRICTORK810353 · LZN | 510(k) clearances |
| Feb 12, 1981 | AGINSKY NAILK803106 · HSB | 510(k) clearances |
| Jan 8, 1981 | FERNORAL HIP PROSTHESISK803074 · JDI | 510(k) clearances |
| Dec 16, 1980 | ORTRON 90* HIP PROSTHESISK802627 · JDI | 510(k) clearances |
| Dec 10, 1980 | ORTHOFIX AXIALEXTERNAL FIXATION SYS.K802814 · 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
