Sprintray, Inc.
Sprintray, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 15, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260661 | Midas Restore | Apr 15, 2026 |
| K250617 | Apex Flex | Apr 29, 2025 |
| K242559 | Digital Temp | Nov 26, 2024 |
| K242277 | Crown HT | Oct 1, 2024 |
| K230445 | OnX Tough | Jul 14, 2023 |
| K222623 | Digital Crown | Dec 14, 2022 |
| K221678 | SprintRay High Impact Denture Base | Nov 10, 2022 |
| K220979 | SprintRay Denture Base | Sep 14, 2022 |
| K212448 | NightGuard Flex | Nov 12, 2021 |