Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Vident — Predicate Candidate Screening

36 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

97 daysmedian FDA review time

405 days90th percentile

36clearances measured

K-number	Device	Applicant	Decided	Review days
K063768	TITANIUM SCALLOPED ABUTMENT	Vident	2007-06-27	189
K060441	VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8,	Vident	2006-04-27	65
K052710	VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, M	Vident	2006-01-13	106
K052130	VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40	Vident	2005-08-15	10
K050362	VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)	Vident	2005-03-15	29
K022996	VITA IN-CERAM YZ CUBES FOR CEREC	Vident	2002-10-09	30
K012473	VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY	Vident	2002-09-11	405
K000597	VITA RESPONSE	Vident	2000-05-17	85
K990367	PDQ AND PDQ-TI ABUTMENT	Vident	1999-04-21	75
K984198	WIDE BODY ABUTMENTS	Vident	1999-02-18	86
K982664	VITA TITANIUM PORCELAIN	Vident	1998-08-02	2
K962333	V.R.S. DENTURE RESIN MATERIAL	Vident	1996-08-07	51
K961434	VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM	Vident	1996-07-08	84
K960480	IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013	Vident	1996-03-15	42
K955406	SCAN WHITE 12 ML	Vident	1995-12-28	31
K951183	IN-CERAM SPINELL	Vident	1995-05-02	47
K923395	VIDENT IMPAC IMPLANT ACCESSORIES	Vident	1994-11-22	865
K940998	IMPAC TORQUE WRENCH	Vident	1994-11-21	262
K941247	VIDENT IMPAC INFINITE POSITION ABUTMENT	Vident	1994-11-21	251
K932893	VIDENT 500 ALLOY AND VIDENT 550 BE ALLOY	Vident	1994-03-28	291
K934195	VITA CELAY BLANKS AND VITA CELAY OPTIMIZER	Vident	1994-03-18	204
K931089	VGA-50 GOLD ALLOY	Vident	1993-05-25	83
K931090	PALLADIUS-6 ALLOY SEMI-PRECIOUS ALLOY	Vident	1993-05-25	83
K925713	VITA CEREC DUO CEMENT	Vident	1993-02-17	97
K921623	VITADUR ALPHA PORCELAIN	Vident	1992-07-02	87
K913644	VITA IN-CERAM	Vident	1992-06-22	311
K921474	VITA OMEGA PORCELAIN	Vident	1992-06-18	80
K914476	VITAPAN ACRYLIC DENTURE TEETH	Vident	1992-03-02	146
K895901	VITA CEREC SET AND VITA CEREC BLOCS	Vident	1992-01-17	833
K904391	VIDENT IMPAC IMPLANT ACCESSORIES	Vident	1991-12-09	440
K902863	PALLADIUS-V AND PALLADIUS-AG SEMI-PRECIOUS ALLOY	Vident	1990-10-24	118
K901862	VMK 68 AND VMK 68N DENTAL PORCELAIN KIT	Vident	1990-10-10	169
K901982	VITACHROM-L DENTAL PORCELAIN KIT	Vident	1990-10-05	156
K902105	VITADUR-N DENTAL PORCELAIN KIT	Vident	1990-10-05	150
K902200	VITA HI-CERAM	Vident	1990-10-05	142
K903008	VIDENT 90 ALLOY AND VIDENT 95 ALLOY	Vident	1990-09-06	57

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda