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OPTIBOND SOLO PLUS ACTIVATOR

Page Type
Cleared 510(K)
510(k) Number
K012082
510(k) Type
Traditional
Applicant
SYBRON DENTAL SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2001
Days to Decision
79 days
Submission Type
Summary

OPTIBOND SOLO PLUS ACTIVATOR

Page Type
Cleared 510(K)
510(k) Number
K012082
510(k) Type
Traditional
Applicant
SYBRON DENTAL SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2001
Days to Decision
79 days
Submission Type
Summary