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BLUEPHASE 16I

Page Type
Cleared 510(K)
510(k) Number
K051782
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2005
Days to Decision
81 days
Submission Type
Statement

BLUEPHASE 16I

Page Type
Cleared 510(K)
510(k) Number
K051782
510(k) Type
Traditional
Applicant
IVOCLAR VIVADENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2005
Days to Decision
81 days
Submission Type
Statement