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 DowLabelled 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 Dow Corning Wright with 74 510(k) clearances. The most recent is a 510(k) clearance dated Sep 7, 1994: ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT.
| Date | Record | Source |
|---|---|---|
| Sep 7, 1994 | ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENTK932210 · JWH | 510(k) clearances |
| Jun 30, 1994 | ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENTK932911 · JWH | 510(k) clearances |
| Jun 3, 1994 | LACEY ALL POLYETHYLENE TIBIAL COMPONENTK934354 · JWH | 510(k) clearances |
| May 27, 1994 | SLT FEMORAL HEADK932222 · LZO | 510(k) clearances |
| Feb 16, 1994 | ORTHOLOC ADVANTIM TIBIAL BASE COMPONENTK932858 · JWH | 510(k) clearances |
| Nov 30, 1993 | ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREEK930228 · JWH | 510(k) clearances |
| Aug 24, 1993 | LACEY REVISION FEMORAL COMPONENTK925900 · JWH | 510(k) clearances |
| Aug 6, 1993 | ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMPK930189 · JWH | 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
