BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LimFlow Inc.

    Reg #: 3023527320 · FEI: 3023527320 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    LimFlow Inc.
    Registration Number
    3023527320
    FEI Number
    3023527320
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    6001 Oak Canyon, Suite 100
    City
    Irvine
    State
    CA
    ZIP
    92618
    Country
    US

    Regulatory Submissions

    510(k) Number
    K260188
    PMA Number
    P220025

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Stent Graft, Infrapopliteal, Venous Arterialization QWN
    Valvulotome MGZ
    Catheter For Crossing Total Occlusions PDU
    Device, Percutaneous Retrieval MMX

    Proprietary Names

    LimFlow Extension Stent Graft LimFlow System LimFlow Crossing Stent Graft LimFlow Vector LimFlow ARC LimFlow V-Ceiver

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility