Neuroone Medical Technologies Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251243 | OneRF Trigeminal Nerve Radiofrequency Probes | August 15, 2025 |
| K231675 | OneRF Ablation System | December 6, 2023 |
| K222404 | Evo® sEEG System | October 20, 2022 |
| K211367 | Evo sEEG System | September 1, 2021 |