Kerr Dental Materials Center is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kerr Dental Materials Center - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Kerr Dental Materials Center has 17 FDA 510(k) cleared dental devices. Based in Orange, US.
Historical record: 17 cleared submissions from 1996 to 2005.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kerr Dental Materials Center
17 devices
Cleared
Aug 11, 2005
BIOPLANT
Dental
114d
Cleared
Jul 02, 2003
OPTIBOND FL
Dental
56d
Cleared
May 06, 2003
BELLEGLASS POINT 4
Dental
67d
Cleared
Apr 19, 2002
XR PRIMER 2
Dental
80d
Cleared
Mar 15, 2002
BELLEGLASS HP MODELING GEL
Dental
56d
Cleared
Feb 22, 2002
OPTIBOND SOLO PLUS 4
Dental
78d
Cleared
Feb 22, 2002
TEMPHASE
Dental
43d
Cleared
Oct 29, 2001
BELLEGLASS HP OPAQUE 2
Dental
18d
Cleared
Oct 23, 2001
POINT 4 FLOWABLE 2
Dental
18d
Cleared
Sep 06, 2001
OPTIBOND SOLO PLUS 3
Dental
79d
Cleared
Apr 28, 2000
EZ CONNECT RESIN
Dental
84d
Cleared
Apr 14, 2000
EZ CONNECT
Dental
71d
Cleared
Aug 27, 1999
BELLEGLAZE
Dental
70d
Cleared
Oct 28, 1998
ELAN-2
Dental
55d
Cleared
Oct 03, 1997
TEMP BOND CLEAR
Dental
63d
Cleared
Aug 01, 1996
KERR ADVANCED ADHESIVE
Dental
35d
Cleared
Jan 23, 1996
OPAKER
Dental
63d