Etex Corp. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Etex Corp. has 17 FDA 510(k) cleared orthopedic devices. Based in Cambridge, US.
Historical record: 17 cleared submissions from 1994 to 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Dec 21, 2010
CARRIGEN
Dental
266d
Cleared
Jul 01, 2010
GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN
Orthopedic
27d
Cleared
Feb 18, 2010
CARRIGEN
Orthopedic
105d
Cleared
Dec 23, 2009
ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
Dental
195d
Cleared
Nov 02, 2009
ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
Orthopedic
152d
Cleared
Sep 18, 2009
EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE
Orthopedic
172d
Cleared
Mar 24, 2009
EQUIVABONE
Orthopedic
46d
Cleared
Feb 20, 2009
GAMMA-BSM, BETA-BSM
Orthopedic
18d
Cleared
Apr 28, 2008
CAP PLUS, EQUIVABONE, CAP/DBM
Orthopedic
81d
Cleared
Nov 19, 2007
CAP PLUS
Orthopedic
411d
Cleared
Oct 23, 2007
A-BSM BONE SUBSTITUTE MATERIAL
Orthopedic
35d
Cleared
Sep 26, 2007
OSSIFUSE BONE SUBSTITUTE MATERIAL
Orthopedic
35d
Cleared
Jun 28, 2007
OSSIPRO BONE SUBSTITUTE MATERIAL
Orthopedic
296d
Cleared
Dec 02, 2003
CAP3 BONE SUBSTITUTE MATERIAL
Orthopedic
63d
Cleared
Oct 24, 2003
CAP BONE SUBSTITUTE MATERIAL
Neurology
91d
Cleared
Nov 25, 1998
BSM- BONE SUBSTITUTE MATERIAL
Neurology
89d
Cleared
Aug 05, 1997
BSM BONE SUBSTITUTE MATERIAL KIT
Dental
403d
Cleared
Jul 22, 1994
ETEX HA HIP REPLACEMENT SYSTEM
Orthopedic
234d