Nanospectra Biosciences, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243701 | AuroLase® System | July 2, 2025 |
| K202953 | Aurolase Therapy, Laser Delivery Device (LDD) | October 3, 2022 |