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LuxCreo Clear Aligner System

Page Type
Cleared 510(K)
510(k) Number
K212680
510(k) Type
Traditional
Applicant
Luxcreo Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2022
Days to Decision
280 days
Submission Type
Summary

LuxCreo Clear Aligner System

Page Type
Cleared 510(K)
510(k) Number
K212680
510(k) Type
Traditional
Applicant
Luxcreo Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2022
Days to Decision
280 days
Submission Type
Summary