Vident
Vident has 0 FDA recalls, 0 inspections, 36 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Jun 27, 2007
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 36 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 27, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K063768 | TITANIUM SCALLOPED ABUTMENT | Jun 27, 2007 |
| K060441 | VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX… | Apr 27, 2006 |
| K052710 | VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX… | Jan 13, 2006 |
| K052130 | VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40 | Aug 15, 2005 |
| K050362 | VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES) | Mar 15, 2005 |
| K022996 | VITA IN-CERAM YZ CUBES FOR CEREC | Oct 9, 2002 |
| K012473 | VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT | Sep 11, 2002 |
| K000597 | VITA RESPONSE | May 17, 2000 |
| K990367 | PDQ AND PDQ-TI ABUTMENT | Apr 21, 1999 |
| K984198 | WIDE BODY ABUTMENTS | Feb 18, 1999 |
| K982664 | VITA TITANIUM PORCELAIN | Aug 2, 1998 |
| K962333 | V.R.S. DENTURE RESIN MATERIAL | Aug 7, 1996 |
| K961434 | VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM | Jul 8, 1996 |
| K960480 | IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 | Mar 15, 1996 |
| K955406 | SCAN WHITE 12 ML | Dec 28, 1995 |
| K951183 | IN-CERAM SPINELL | May 2, 1995 |
| K923395 | VIDENT IMPAC IMPLANT ACCESSORIES | Nov 22, 1994 |
| K940998 | IMPAC TORQUE WRENCH | Nov 21, 1994 |
| K941247 | VIDENT IMPAC INFINITE POSITION ABUTMENT | Nov 21, 1994 |
| K932893 | VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY | Mar 28, 1994 |