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.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Etex Corporation with 25 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2024: EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 18, 2024 | EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )K243609 · MQV | 510(k) clearances |
| Aug 31, 2018 | CarriGen PFK182107 · MQV | 510(k) clearances |
| Feb 20, 2015 | CARRICELLK132868 · MQV | 510(k) clearances |
| Jul 9, 2014 | ETEX MIXING AND DELIVERY SYSTEMK141245 · FMF | 510(k) clearances |
| Dec 21, 2010 | CARRIGENK100883 · LYC | 510(k) clearances |
| Dec 3, 2010 | GAMMA-BSM; BETA-BSM; EQUIVABONEK102812 · LYC | 510(k) clearances |
| Jul 1, 2010 | GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGENK101557 · MQV | 510(k) clearances |
| Feb 18, 2010 | CARRIGENK093447 · MQV | 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
