Luminopia, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2025-04-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243819 | Luminopia | QQU | 2025-04-09 | View |
| 510(k) | K233720 | Luminopia | QQU | 2024-08-08 | View |
| 510(k) | K221659 | Luminopia One | QQU | 2022-11-04 | View |
No matching devices.