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FDA 510(k) Applications Submitted by SprintRay Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230445
02/21/2023
OnX Tough
SprintRay Inc.
K221678
06/09/2022
SprintRay High Impact Denture Base
SprintRay Inc.
K222623
08/31/2022
Digital Crown
SprintRay Inc.
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