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., part of Zimmer BiometLabelled by claude-sonnet-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 Orthomet with 60 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 1995: ORTHOMET HMC FEMORAL STEM COMPONENT.
| Jun 7, 1995 | ORTHOMET HMC FEMORAL STEM COMPONENTK936310 · LPH | 510(k) clearances |
| May 30, 1995 | ORTHOMET TITANIUM HYBRID FEMORAL STEMK945783 · JDG | 510(k) clearances |
| Apr 26, 1995 | ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYK943873 · LXH | 510(k) clearances |
| Dec 28, 1994 | ORTHOMET RESURFACING FEMORAL COMPONENTK944752 · KXA | 510(k) clearances |
| Nov 30, 1994 | PERFECTA TOTAL HIP SYSTEM COATED COCR FEMORAL STEMK930771 · JDI | 510(k) clearances |
| Oct 18, 1994 | AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSERK926334 · JWH | 510(k) clearances |
| Oct 14, 1994 | ORTHOMET ACETABULAR CUP SYSTEMK931333 · LPH | 510(k) clearances |
| Oct 14, 1994 | ORTHOMET LHMC FEMORAL STEMK931678 · HMC | 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
