# Arbor Endovascular, LLC

- Location (FDA's records): San Jose, CA
- FDA decisions: 5 (2025–2026): 5 510(k) clearances
- Product codes: MOF (5)
- 510(k) review time since 2016: median 30 days, against 192 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 5 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stryker Neurovascular: 1 (https://510kreport.com/company/stryker-neurovascular)

## Its most-cited devices
- K253168: 0.014” Willow Guidewire (2025), cited by 2
- K243756: 0.014” Willow Guidewire (2025), cited by 1
- K260130: Willow 18 Guidewire (2026), cited by 1

## Recent decisions
- K262424: Willow 12 Guidewire (Aug 14, 2026)
- K260537: Willow 24 Guidewire (Mar 19, 2026)
- K260130: Willow 18 Guidewire (Feb 13, 2026)
- K253168: 0.014” Willow Guidewire (Nov 26, 2025)
- K243756: 0.014” Willow Guidewire (Jul 17, 2025)

Source page: https://510kreport.com/company/arbor-endovascular