ClearanceBrief
Company ยท US

Ab Ardent

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2013. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EBFMaterial, Tooth Shade, Resin6
EJJAlloy, Amalgam5
EIHPowder, Porcelain1
EMACement, Dental1
KLEAgent, Tooth Bonding, Resin1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 14, 2013K131753MERIDIAN
Ab Ardent
EBF
Feb 20, 2013K123613SYNSPAR ADVANCED
Ardent, Inc.
EIH
Jul 20, 2004K040465LATIT FLOW
Ab Ardent
EBF
Nov 25, 2002K022971MICROHYBRID 11
Ab Ardent
EBF
Nov 22, 2002K022975ETCHING 15
Ab Ardent
EBF
Nov 22, 2002K022974MICROHYBRID 12
Ab Ardent
EBF
Nov 22, 2002K022973ADHESIVE 14
Ab Ardent
KLE
Nov 22, 2002K022972MICROFILL 13
Ab Ardent
EBF
May 7, 2002K020452HIGH SILVER CONVENTIONAL
Ab Ardent
EJJ
Aug 16, 2001K011801FUTURA TOPCAP NON GAMMA-2
Ab Ardent
EJJ
Sep 17, 1999K991974FUTURA GLASS IONOMER SILVER REINFORCED
Ab Ardent
EMA
Aug 24, 1998K982460VIVACAP HR
Ab Ardent
EJJ
Aug 24, 1998K982458VIVALLOY HR
Ab Ardent
EJJ
Aug 24, 1998K982456AMALCAP PLUS
Ab Ardent
EJJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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