FDA 510(k) Applications Submitted by SprintRay Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220979 | 04/04/2022 | SprintRay Denture Base | SprintRay Inc |
| K212448 | 08/05/2021 | NightGuard Flex | SprintRay Inc |
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