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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