Arbor Endovascular, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arbor Endovascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: Willow 24 Guidewire, Willow 18 Guidewire, 0.014” Willow Guidewire
4
Total
4
Cleared
0
Denied
Arbor Endovascular, LLC has 4 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Mar 2026. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Arbor Endovascular, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Fabrica Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Arbor Endovascular, LLC
4 devices