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VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012473
510(k) Type
Traditional
Applicant
VIDENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2002
Days to Decision
405 days
Submission Type
Statement

VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012473
510(k) Type
Traditional
Applicant
VIDENT
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2002
Days to Decision
405 days
Submission Type
Statement