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 14, 2026, FDA's public records list Metagen with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1998: METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM.
| Dec 30, 1998 | METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEMK983976 · JDQ | 510(k) clearances |
| May 18, 1998 | SEGMENTAL DEFECT REPLACEMENT SYSTEMK980609 · HSB | 510(k) clearances |
| Apr 3, 1998 | ACTIVELOCK MODULAR FEMORAL HIP SYSTEMK980020 · LPH | 510(k) clearances |
| Mar 21, 1997 | METAGEN ALL POLY ACETABULAR CUP SYSTEMK964003 · JDI | 510(k) clearances |
| Feb 12, 1997 | METAGEN HIGH TIBIAL OSTEOTOMY SYSTEMK963700 · HRS | 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
