FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VITA TITANIUM PORCELAIN

K Number: K982664 · Decision Aug 2, 1998
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
36
Review Days
2

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Basic Information

Device Name
VITA TITANIUM PORCELAIN
K Number
K982664
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vident
Date Received
July 31, 1998
Decision Date
August 2, 1998
Product Code
EIH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EIH Powder, Porcelain

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EIH), ordered by most recent decision date.

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Other Clearances by Vident

K Number Device Name
K063768 TITANIUM SCALLOPED ABUTMENT
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
K052710 VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,
K052130 VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40
K050362 VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)
K022996 VITA IN-CERAM YZ CUBES FOR CEREC
K012473 VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT
K000597 VITA RESPONSE
K990367 PDQ AND PDQ-TI ABUTMENT
K984198 WIDE BODY ABUTMENTS
Search all 36 clearances from Vident →