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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