Kerr Corporation (Danbury)

FDA Regulatory Profile

Kerr Corporation (Danbury) appears in FDA public data with 0 recalls, 32 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 18, 2005.

Summary

Total Recalls
0
510(k) Clearances
32
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K051545L.E. DEMETRON IIJuly 18, 2005
K020091OPTILUX 501March 21, 2002
K951663TYTIN RJune 6, 1995
K951511TYTIN ADMIXMay 2, 1995
K942480M4 CONTRA-ANGLE HANDPIECEJanuary 27, 1995
K940513OPTIBONDApril 15, 1994
K935535TYTINMarch 11, 1994
K934690KERR OPTIBOND, MODIFICATIONDecember 30, 1993
K923546OPTIBONDSeptember 29, 1992
K915847AUTOMIX DENTAL AMALGAMATORMarch 2, 1992
K904756MATRICSMarch 15, 1991
K904482STAT.BR TMNovember 29, 1990
K894219TEMP BOND NESeptember 18, 1989
K880250KERR XR BONDJune 1, 1988
K880251KERR XR IONOMERJune 1, 1988
K880685PORCELITE DUAL CURE CEMENTMay 11, 1988
K880684XR PRIMERMay 11, 1988
K872147KERR CAVALITEAugust 26, 1987
K860346KERR PORCELITEMarch 25, 1986
K860532KERR POL-E-LASTIC DENTAL IMPRESSION MATERIALMarch 20, 1986