Not currently registered with FDA under this name

Vident

Brea, CA, United States. Named as applicant on 36 dental 510(k) clearances between 1990 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 361990–2007
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Vident as the applicant.

Decided	510(k)	Device	Device type
27 Jun 2007	K063768	TITANIUM SCALLOPED ABUTMENT	NHA Endosseous Dental Implant Abutment
27 Apr 2006	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 Porcelain Powder
13 Jan 2006	K052710	VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,	EIH Porcelain Powder
15 Aug 2005	K052130	VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40	EIH Porcelain Powder
15 Mar 2005	K050362	VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)	EIH Porcelain Powder
9 Oct 2002	K022996	VITA IN-CERAM YZ CUBES FOR CEREC	EIH Porcelain Powder
11 Sep 2002	K012473	VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT	DZE Root-Form Endosseous Implant
17 May 2000	K000597	VITA RESPONSE	EIH Porcelain Powder
21 Apr 1999	K990367	PDQ AND PDQ-TI ABUTMENT	DZE Root-Form Endosseous Implant
18 Feb 1999	K984198	WIDE BODY ABUTMENTS	DZE Root-Form Endosseous Implant
2 Aug 1998	K982664	VITA TITANIUM PORCELAIN	EIH Porcelain Powder
7 Aug 1996	K962333	V.R.S. DENTURE RESIN MATERIAL	EBI Rebasing Repairing Relining Denture Resin
8 Jul 1996	K961434	VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM	EBF Resin Tooth Shade Material
15 Mar 1996	K960480	IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013	ELL Porcelain Teeth
28 Dec 1995	K955406	SCAN WHITE 12 ML	ELW Impression Material
2 May 1995	K951183	IN-CERAM SPINELL	EIH Porcelain Powder
22 Nov 1994	K923395	VIDENT IMPAC IMPLANT ACCESSORIES	DZE Root-Form Endosseous Implant
21 Nov 1994	K941247	VIDENT IMPAC INFINITE POSITION ABUTMENT	DZE Root-Form Endosseous Implant
21 Nov 1994	K940998	IMPAC TORQUE WRENCH	DZE Root-Form Endosseous Implant
28 Mar 1994	K932893	VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY	EJH Base Metal Alloy
18 Mar 1994	K934195	VITA CELAY BLANKS AND VITA CELAY OPTIMIZER	EIH Porcelain Powder
25 May 1993	K931090	PALLADIUS-6 ALLOY SEMI-PRECIOUS ALLOY	EJT Gold-Based Noble Metal Alloy
25 May 1993	K931089	VGA-50 GOLD ALLOY	EJT Gold-Based Noble Metal Alloy
17 Feb 1993	K925713	VITA CEREC DUO CEMENT	EMA Dental Cement
2 Jul 1992	K921623	VITADUR ALPHA PORCELAIN	EIH Porcelain Powder
22 Jun 1992	K913644	VITA IN-CERAM	EIH Porcelain Powder
18 Jun 1992	K921474	VITA OMEGA PORCELAIN	EIH Porcelain Powder
2 Mar 1992	K914476	VITAPAN ACRYLIC DENTURE TEETH	ELM Teeth Plastic Denture
17 Jan 1992	K895901	VITA CEREC SET AND VITA CEREC BLOCS	ELW Impression Material
9 Dec 1991	K904391	VIDENT IMPAC IMPLANT ACCESSORIES	DZE Root-Form Endosseous Implant
24 Oct 1990	K902863	PALLADIUS-V AND PALLADIUS-AG SEMI-PRECIOUS ALLOY	EJT Gold-Based Noble Metal Alloy
10 Oct 1990	K901862	VMK 68 AND VMK 68N DENTAL PORCELAIN KIT	EIH Porcelain Powder
5 Oct 1990	K902200	VITA HI-CERAM	EIH Porcelain Powder
5 Oct 1990	K902105	VITADUR-N DENTAL PORCELAIN KIT	EIH Porcelain Powder
5 Oct 1990	K901982	VITACHROM-L DENTAL PORCELAIN KIT	EIH Porcelain Powder
6 Sep 1990	K903008	VIDENT 90 ALLOY AND VIDENT 95 ALLOY	EJH Base Metal Alloy

Some of these clearances are listed with FDA today by another company: Vita Zahnfabrik H. Rauter GmbH & Co. Kg. (18), Vita Tesco (1).

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.