Etex Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Etex Corporation has 5 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Latest FDA clearance: Dec 2024. Active since 2010. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Etex Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Etex Corporation
5 devices
Cleared
Dec 18, 2024
EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )
Orthopedic
26d
Cleared
Aug 31, 2018
CarriGen PF
Orthopedic
28d
Cleared
Feb 20, 2015
CARRICELL
Orthopedic
525d
Cleared
Jul 09, 2014
ETEX MIXING AND DELIVERY SYSTEM
General Hospital
56d
Cleared
Dec 03, 2010
GAMMA-BSM
Dental
66d