Company · US
Arbor Endovascular, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2025 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (4 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| MOF | Guide, Wire, Catheter, Neurovasculature | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 14, 2026 | K262424 | Willow 12 Guidewire Arbor Endovascular, LLC | MOF |
| Mar 19, 2026 | K260537 | Willow 24 Guidewire Arbor Endovascular, LLC | MOF |
| Feb 13, 2026 | K260130 | Willow 18 Guidewire Arbor Endovascular, LLC | MOF |
| Nov 26, 2025 | K253168 | 0.014 Willow Guidewire Arbor Endovascular, LLC | MOF |
| Jul 17, 2025 | K243756 | 0.014 Willow Guidewire Arbor Endovascular, LLC | MOF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||