FDA 510(k) Applications Submitted by VIDENT
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K022996 |
09/09/2002 |
VITA IN-CERAM YZ CUBES FOR CEREC |
VIDENT |
| K990367 |
02/05/1999 |
PDQ AND PDQ-TI ABUTMENT |
VIDENT |
| K050362 |
02/14/2005 |
VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES) |
VIDENT |
| K060441 |
02/21/2006 |
VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98 |
VIDENT |
| K000597 |
02/22/2000 |
VITA RESPONSE |
VIDENT |
| K012473 |
08/02/2001 |
VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT |
VIDENT |
| K052130 |
08/05/2005 |
VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40 |
VIDENT |
| K052710 |
09/29/2005 |
VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, |
VIDENT |
| K984198 |
11/24/1998 |
WIDE BODY ABUTMENTS |
VIDENT |
| K063768 |
12/20/2006 |
TITANIUM SCALLOPED ABUTMENT |
VIDENT |
| K960480 |
02/02/1996 |
IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 |
VIDENT |
| K961434 |
04/15/1996 |
VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM |
VIDENT |
| K962333 |
06/17/1996 |
V.R.S. DENTURE RESIN MATERIAL |
VIDENT |
| K982664 |
07/31/1998 |
VITA TITANIUM PORCELAIN |
VIDENT |
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