Data / Medical devices / United States / Arbor Endovascular
Arbor Endovascular: FDA-registered device maker in San Jose, CA, United States, 5 510(k) clearances
Arbor Endovascular is registered with the FDA (registration 3039642752) in San Jose, CA, United States. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated August 14, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039642752
- Address
- 2345 Bering Dr, San Jose, CA, United States, 95131
- Owner or operator
- Arbor Endovascular (10093944)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- August 15, 2025
- Registered through
- 2026
- Brand names listed
- 014" Willow Guidewire, 14 Willow Wire, Cypress 14 Guidewire, Cypress 18 Guidewire, Willow 12 Guidewire, Willow 14 Guidewire, Willow 18 Guidewire, Willow 24 Guidewire
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Guide, Wire, Catheter, Neurovasculature | MOF | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Wire, Guide, Catheter | DQX | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 14, 2026 | K262424 | Willow 12 Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| March 19, 2026 | K260537 | Willow 24 Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| February 13, 2026 | K260130 | Willow 18 Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| November 26, 2025 | K253168 | 0.014 Willow Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
| July 17, 2025 | K243756 | 0.014 Willow Guidewire | MOF | Substantially Equivalent | Arbor Endovascular, LLC | accessdata.fda.gov |
Compare with other makers
Updated August 14, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.