Luminance Medical Ventures, 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 |
|---|
| K251973 | Luminance Red Cold Sore Device (TN1927G) | September 23, 2025 |
| K220729 | The Luminance RED Acne Device | June 9, 2022 |