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Ab Ardent

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131753MERIDIANNovember 14, 2013
K040465LATIT FLOWJuly 20, 2004
K022971MICROHYBRID 11November 25, 2002
K022972MICROFILL 13November 22, 2002
K022975ETCHING 15November 22, 2002
K022973ADHESIVE 14November 22, 2002
K022974MICROHYBRID 12November 22, 2002
K020452HIGH SILVER CONVENTIONALMay 7, 2002
K011801FUTURA TOPCAP NON GAMMA-2August 16, 2001
K991974FUTURA GLASS IONOMER SILVER REINFORCEDSeptember 17, 1999
K982458VIVALLOY HRAugust 24, 1998
K982460VIVACAP HRAugust 24, 1998
K982456AMALCAP PLUSAugust 24, 1998