Vident is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vident - FDA 510(k) Cleared Devices
36
Total
36
Cleared
0
Denied
Vident has 36 FDA 510(k) cleared dental devices. Based in Baldwin Park, US.
Historical record: 36 cleared submissions from 1990 to 2007.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vident
36 devices
Cleared
Jun 27, 2007
TITANIUM SCALLOPED ABUTMENT
Dental
189d
Cleared
Apr 27, 2006
VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX
Dental
65d
Cleared
Jan 13, 2006
VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX
Dental
106d
Cleared
Aug 15, 2005
VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40
Dental
10d
Cleared
Mar 15, 2005
VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)
Dental
29d
Cleared
Oct 09, 2002
VITA IN-CERAM YZ CUBES FOR CEREC
Dental
30d
Cleared
Sep 11, 2002
VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT
Dental
405d
Cleared
May 17, 2000
VITA RESPONSE
Dental
85d
Cleared
Apr 21, 1999
PDQ AND PDQ-TI ABUTMENT
Dental
75d
Cleared
Feb 18, 1999
WIDE BODY ABUTMENTS
Dental
86d
Cleared
Aug 02, 1998
VITA TITANIUM PORCELAIN
Dental
2d
Cleared
Aug 07, 1996
V.R.S. DENTURE RESIN MATERIAL
Dental
51d