Sensomedical Labs, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253970 | Wovyn Depth Electrode | April 17, 2026 |
| K213170 | SENSOSEEG Depth Electrodes | April 18, 2023 |