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 13, 2026, FDA's public records list Osteo AG with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 30, 1994: OSTEO INTERLOCKING-COMPRESSION NAIL.
| Date | Record | Source |
|---|---|---|
| Jun 30, 1994 | OSTEO INTERLOCKING-COMPRESSION NAILK933340 · HSB | 510(k) clearances |
| Jul 23, 1992 | OSTEO KIRSCHNER WIREK922193 · HTY | 510(k) clearances |
| Jul 23, 1992 | OSTEO FEMORAL NAILK922195 · HSB | 510(k) clearances |
| Jul 23, 1992 | OSTEO STEINMANN PINK922194 · HTY | 510(k) clearances |
| Jul 23, 1992 | OSTEO TIBIA NAILK922196 · HSB | 510(k) clearances |
| Apr 9, 1992 | OSTEO EX-FI-REK920149 · JEC | 510(k) clearances |
| Mar 11, 1992 | OSTEO COMPRESSION HIP SCREWK920037 · HRC | 510(k) clearances |
| Dec 30, 1991 | OSTEO CERCLAGE WIREK914374 · JDQ | 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
