Vident
FDA 510(k) & PMA Approved Devices — 36 products
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Total Devices36
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K063768 | TITANIUM SCALLOPED ABUTMENT | NHA | 2007-06-27 | View |
| 510(k) | K060441 | VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98 | EIH | 2006-04-27 | View |
| 510(k) | K052710 | VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, | EIH | 2006-01-13 | View |
| 510(k) | K052130 | VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40 | EIH | 2005-08-15 | View |
| 510(k) | K050362 | VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES) | EIH | 2005-03-15 | View |
| 510(k) | K022996 | VITA IN-CERAM YZ CUBES FOR CEREC | EIH | 2002-10-09 | View |
| 510(k) | K012473 | VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT | DZE | 2002-09-11 | View |
| 510(k) | K000597 | VITA RESPONSE | EIH | 2000-05-17 | View |
| 510(k) | K990367 | PDQ AND PDQ-TI ABUTMENT | DZE | 1999-04-21 | View |
| 510(k) | K984198 | WIDE BODY ABUTMENTS | DZE | 1999-02-18 | View |
| 510(k) | K982664 | VITA TITANIUM PORCELAIN | EIH | 1998-08-02 | View |
| 510(k) | K962333 | V.R.S. DENTURE RESIN MATERIAL | EBI | 1996-08-07 | View |
| 510(k) | K961434 | VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM | EBF | 1996-07-08 | View |
| 510(k) | K960480 | IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 | ELL | 1996-03-15 | View |
| 510(k) | K955406 | SCAN WHITE 12 ML | ELW | 1995-12-28 | View |
| 510(k) | K951183 | IN-CERAM SPINELL | EIH | 1995-05-02 | View |
| 510(k) | K923395 | VIDENT IMPAC IMPLANT ACCESSORIES | DZE | 1994-11-22 | View |
| 510(k) | K940998 | IMPAC TORQUE WRENCH | DZE | 1994-11-21 | View |
| 510(k) | K941247 | VIDENT IMPAC INFINITE POSITION ABUTMENT | DZE | 1994-11-21 | View |
| 510(k) | K932893 | VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY | EJH | 1994-03-28 | View |
No matching devices.
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