Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Technology with 18 510(k) clearances. The most recent is a 510(k) clearance dated Mar 9, 1994: REPLICA(TM) TOTAL HIP SYSTEM.
| Date | Record | Source |
|---|---|---|
| Mar 9, 1994 | REPLICA(TM) TOTAL HIP SYSTEMK926156 · LPH | 510(k) clearances |
| Sep 23, 1993 | ANATOMICAL TYPE KNEE SYSTEMK922859 · JWH | 510(k) clearances |
| Jul 13, 1993 | TOTAL CONDYLAT TYPE KNEE SYSTEMK922869 · JWH | 510(k) clearances |
| Jun 29, 1993 | OTI ORTHOPEDIC WIRE SYSTEMK925447 · JDQ | 510(k) clearances |
| Jun 17, 1993 | MODIFIED ZICKEL INTRAMEDULLARY ROD SYSTEMK926213 · HSB | 510(k) clearances |
| May 12, 1993 | BIOMETRIC SCREW FIXATION CUPK922861 · JDL | 510(k) clearances |
| Apr 8, 1993 | THREE SPIKE CUPK922870 · GRF | 510(k) clearances |
| Mar 16, 1993 | AMERICANA HIP PROTHESISK922682 · JDG | 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
