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 Biologically Oriented Prostheses with 9 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 2000: WUJIN #3 TIBIAL NAIL.
| Date | Record | Source |
|---|---|---|
| Oct 30, 2000 | WUJIN #3 TIBIAL NAILK002325 · JDS | 510(k) clearances |
| Sep 22, 1999 | BIOPRO RIMMED ACETABULAR COMPOMENTK992144 · LZO | 510(k) clearances |
| Feb 3, 1997 | RIOPRO COBALT TRAPEZIOMETARCARPAL RESURFACING COMPONENTK964472 · KYI | 510(k) clearances |
| Oct 3, 1996 | HORIZON HIP SYSTEMK962769 · LPH | 510(k) clearances |
| Aug 8, 1996 | TOWNLEY TOTAL ELBOW SYSTEMK955916 · JDC | 510(k) clearances |
| Jan 18, 1996 | BIOPRO HEMI-ENDO MODULAR CERAMIC HEADK954768 · LZO | 510(k) clearances |
| Dec 28, 1995 | TOWNLEY ALL POLY ACETABULAR CUPK952731 · JDI | 510(k) clearances |
| Sep 27, 1995 | BIOPRO HEMI-ENDO MODULAR CERAMIC HEADK953045 · LZO | 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
