BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ARBOR ENDOVASCULAR

    Reg #: 3039642752 · FEI: 3039642752 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    2

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    Registration Details

    Registration Name
    ARBOR ENDOVASCULAR
    Registration Number
    3039642752
    FEI Number
    3039642752
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    2345 Bering Dr
    City
    San Jose
    State
    CA
    ZIP
    95131
    Country
    US

    Regulatory Submissions

    510(k) Number
    K260130

    Owner / Operator

    Firm Name
    Arbor Endovascular
    Operator Number
    10093944
    Address
    2345 Bering Drive
    City
    San Jose
    State
    CA
    Postal Code
    95131
    Country
    US
    Correspondent
    Kathy Tansey

    Products

    Device Name Product Code
    Guide, Wire, Catheter, Neurovasculature MOF
    Wire, Guide, Catheter DQX

    Proprietary Names

    Willow 18 Guidewire Willow 14 Guidewire 014" Willow Guidewire 14 Willow Wire Willow 24 Guidewire

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility