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Spark Clear Aligner System

Page Type
Cleared 510(K)
510(k) Number
K203737
510(k) Type
Traditional
Applicant
Ormco Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2021
Days to Decision
90 days
Submission Type
Summary

Spark Clear Aligner System

Page Type
Cleared 510(K)
510(k) Number
K203737
510(k) Type
Traditional
Applicant
Ormco Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2021
Days to Decision
90 days
Submission Type
Summary