Arbor Endovascular, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K260130 | Willow 18 Guidewire | February 13, 2026 |
| K253168 | 0.014 Willow Guidewire | November 26, 2025 |
| K243756 | 0.014 Willow Guidewire | July 17, 2025 |