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 Orthopaedic Innovations, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Apr 15, 2002: ORTHOPAEDIC INNOVATIONS RENEWAL ACETABULAR CUP SYSTEM.
| Apr 15, 2002 | ORTHOPAEDIC INNOVATIONS RENEWAL ACETABULAR CUP SYSTEMK020145 · LPH | 510(k) clearances |
| Dec 4, 1998 | COBRA EXTERNAL FIXATORK983881 · HRS | 510(k) clearances |
| Sep 23, 1996 | PRIME MODULAR ENDO HEADK962646 · KWL | 510(k) clearances |
| Mar 18, 1996 | PRACTIFIX EXTERNAL FIXATION SYSTEMK960014 · KTT | 510(k) clearances |
| Feb 20, 1996 | PRIME CEMENTED CALCAR FEMORAL STEMSK955620 · JDI | 510(k) clearances |
| Jan 26, 1996 | PRIME FEMORAL CEMENT PLUGK955751 · LZN | 510(k) clearances |
| Sep 13, 1995 | PRIME CEMENTED SMALL FEMORAL STEMK953033 · JDI | 510(k) clearances |
| Apr 7, 1995 | PRIME CEMENTED HIP SYSTEMK940328 · JDI | 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
