Kerr Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kerr Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Kerr Corp. has 9 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 9 cleared submissions from 2000 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kerr Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kerr Corp.
9 devices
Cleared
Oct 07, 2009
TAKE 1
Dental
126d
Cleared
Apr 03, 2009
PREMISE MODIFIED
Dental
57d
Cleared
Aug 12, 2008
DMC COMPOSITE
Dental
56d
Cleared
Dec 04, 2007
STANDOUT 2
Dental
78d
Cleared
Nov 10, 2004
DEMETRON IDS CURING LIGHT
Dental
22d
Cleared
Jul 03, 2003
STAND OUT
Dental
52d
Cleared
Feb 04, 2002
DEMETRON LC
Dental
46d
Cleared
Apr 23, 2001
TAKE ONE BITE MODIFIED
Dental
20d
Cleared
Aug 10, 2000
PERMLASTIC 2
Dental
71d