Arbor Endovascular, LLC

Arbor Endovascular, LLC holds 5 FDA 510(k) medical device clearances, first cleared 2025, most recent 2026.

Top product codes for Arbor Endovascular, LLC

MOF — Cardiovascular5 devices

Recent clearances by Arbor Endovascular, LLC

K262424 — Willow 12 GuidewireCode MOF·2026-08-14
K260537 — Willow 24 GuidewireCode MOF·2026-03-19
K260130 — Willow 18 GuidewireCode MOF·2026-02-13
K253168 — 0.014 Willow GuidewireCode MOF·2025-11-26
K243756 — 0.014 Willow GuidewireCode MOF·2025-07-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.