Medical Device Manufacturer · US , Baldwin Park , CA

Vident - FDA 510(k) Cleared Devices

36 submissions · 36 cleared · Since 1990

Recent clearances: TITANIUM SCALLOPED ABUTMENT, VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX, VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX

36

Total

36

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vident Dental ✕

36 devices

1-12 of 36

Cleared Jun 27, 2007

TITANIUM SCALLOPED ABUTMENT

Cleared Apr 27, 2006

VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX

Cleared Jan 13, 2006

VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX

Cleared Aug 15, 2005

VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40

Cleared Mar 15, 2005

VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)

Cleared Oct 09, 2002

VITA IN-CERAM YZ CUBES FOR CEREC

Cleared Sep 11, 2002

VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT

Cleared May 17, 2000

Cleared Apr 21, 1999

PDQ AND PDQ-TI ABUTMENT

Cleared Feb 18, 1999

WIDE BODY ABUTMENTS

Cleared Aug 02, 1998

VITA TITANIUM PORCELAIN

Cleared Aug 07, 1996

V.R.S. DENTURE RESIN MATERIAL