Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Etex Corporation

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest Approval2024-12-18
TypeNumberDevice NameCodeDate
510(k) K243609 EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) MQV 2024-12-18 View
510(k) K182107 CarriGen PF MQV 2018-08-31 View