Vident

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
36
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K063768TITANIUM SCALLOPED ABUTMENTJune 27, 2007
K060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VApril 27, 2006
K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VIJanuary 13, 2006
K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40August 15, 2005
K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)March 15, 2005
K022996VITA IN-CERAM YZ CUBES FOR CERECOctober 9, 2002
K012473VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENTSeptember 11, 2002
K000597VITA RESPONSEMay 17, 2000
K990367PDQ AND PDQ-TI ABUTMENTApril 21, 1999
K984198WIDE BODY ABUTMENTSFebruary 18, 1999
K982664VITA TITANIUM PORCELAINAugust 2, 1998
K962333V.R.S. DENTURE RESIN MATERIALAugust 7, 1996
K961434VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEMJuly 8, 1996
K960480IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013March 15, 1996
K955406SCAN WHITE 12 MLDecember 28, 1995
K951183IN-CERAM SPINELLMay 2, 1995
K923395VIDENT IMPAC IMPLANT ACCESSORIESNovember 22, 1994
K940998IMPAC TORQUE WRENCHNovember 21, 1994
K941247VIDENT IMPAC INFINITE POSITION ABUTMENTNovember 21, 1994
K932893VIDENT 500 ALLOY AND VIDENT 550 BE ALLOYMarch 28, 1994