Nanospectra Biosciences, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2025-07-02
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K243701 | AuroLase® System | GEX | 2025-07-02 | View |
| 510(k) | K202953 | Aurolase Therapy, Laser Delivery Device (LDD) | GEX | 2022-10-03 | View |
No matching devices.