Sprintray, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
Total Devices9
Categories4
Latest Approval2026-04-15
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K260661 | Midas Restore | 2026-04-15 | View | |
| 510(k) | K250617 | Apex Flex | EBI | 2025-04-29 | View |
| 510(k) | K242559 | Digital Temp | EBG | 2024-11-26 | View |
| 510(k) | K242277 | Crown HT | EBF | 2024-10-01 | View |
| 510(k) | K230445 | OnX Tough | EBI | 2023-07-14 | View |
| 510(k) | K222623 | Digital Crown | EBF | 2022-12-14 | View |
| 510(k) | K221678 | SprintRay High Impact Denture Base | EBI | 2022-11-10 | View |
| 510(k) | K220979 | SprintRay Denture Base | EBI | 2022-09-14 | View |
| 510(k) | K212448 | NightGuard Flex | MQC | 2021-11-12 | View |
No matching devices.