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FDA 510(k) Applications Submitted by AB ARDENT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020452
02/11/2002
HIGH SILVER CONVENTIONAL
AB ARDENT
K040465
02/23/2004
LATIT FLOW
AB ARDENT
K011801
06/08/2001
FUTURA TOPCAP NON GAMMA-2
AB ARDENT
K991974
06/11/1999
FUTURA GLASS IONOMER SILVER REINFORCED
AB ARDENT
K982456
07/15/1998
AMALCAP PLUS
AB ARDENT
K982458
07/15/1998
VIVALLOY HR
AB ARDENT
K982460
07/15/1998
VIVACAP HR
AB ARDENT
K022971
09/06/2002
MICROHYBRID 11
AB ARDENT
K022972
09/06/2002
MICROFILL 13
AB ARDENT
K022973
09/06/2002
ADHESIVE 14
AB ARDENT
K022974
09/06/2002
MICROHYBRID 12
AB ARDENT
K022975
09/06/2002
ETCHING 15
AB ARDENT
K131753
06/14/2013
MERIDIAN
AB ARDENT
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