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EOS INLAY MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K896469
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1990
Days to Decision
193 days

EOS INLAY MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K896469
510(k) Type
Traditional
Applicant
IVOCLAR NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/1990
Days to Decision
193 days