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SprintRay High Impact Denture Base

Page Type
Cleared 510(K)
510(k) Number
K221678
510(k) Type
Traditional
Applicant
SprintRay Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2022
Days to Decision
154 days
Submission Type
Summary

SprintRay High Impact Denture Base

Page Type
Cleared 510(K)
510(k) Number
K221678
510(k) Type
Traditional
Applicant
SprintRay Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2022
Days to Decision
154 days
Submission Type
Summary