Medical Device Manufacturer · US , San Jose , CA

Arbor Endovascular, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2025

Recent clearances: Willow 12 Guidewire, Willow 24 Guidewire, Willow 18 Guidewire

View 5 510(k) Devices ↓ Official Website
5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Arbor Endovascular, LLC Neurology ✕

5 devices
1-5 of 5
Cleared Aug 14, 2026
Willow 12 Guidewire
K262424 · MOF
Neurology · 29d
Cleared Mar 19, 2026
Willow 24 Guidewire
K260537 · MOF
Neurology · 30d
Cleared Feb 13, 2026
Willow 18 Guidewire
K260130 · MOF
Neurology · 28d
Cleared Nov 26, 2025
0.014” Willow Guidewire
K253168 · MOF
Neurology · 61d
Cleared Jul 17, 2025
0.014” Willow Guidewire
K243756 · MOF
Neurology · 223d
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