Endovascular Engineering, 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 |
|---|
| K252956 | Helo Thrombectomy System | December 18, 2025 |
| K223891 | Cobra Catheter System | February 15, 2023 |