Arbor Endovascular, LLC

FDA Regulatory Profile

Arbor Endovascular, LLC appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 19, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260537Willow 24 GuidewireMarch 19, 2026
K260130Willow 18 GuidewireFebruary 13, 2026
K2531680.014” Willow GuidewireNovember 26, 2025
K2437560.014” Willow GuidewireJuly 17, 2025