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SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844349
510(k) Type
Traditional
Applicant
IVOCLAR USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1984
Days to Decision
24 days

SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844349
510(k) Type
Traditional
Applicant
IVOCLAR USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1984
Days to Decision
24 days