BEUDAMED
    FDA Registration Active 🇺🇸 United States

    XR90 System, LOGIQ

    Reg #: 3030598507 · FEI: 3030598507 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MediView XR Minnesota Office
    Registration Number
    3030598507
    FEI Number
    3030598507
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1970 Oakcrest Ave, Suite 215
    City
    Roseville
    State
    MN
    ZIP
    55113
    Country
    US

    Regulatory Submissions

    510(k) Number
    K223125

    Owner / Operator

    Firm Name
    MediView XR
    Operator Number
    10081343
    Address
    10000 Cedar Ave, STE GCIC2-153
    City
    Cleveland
    State
    OH
    Postal Code
    44106
    Country
    US
    Correspondent
    Adam Cargill

    Products

    Device Name Product Code
    System, Image Processing, Radiological LLZ

    Proprietary Names

    XR90 System, LOGIQ XR90 System, Vivid Registration Marker Kit, Sterile, Single EM Probe Bracket Kit, C1-5, Single EM Probe Bracket Kit, C1-6, Single XR90 System, LOGIQ, Upgrade Kit Triangle Template Kit XR90 System, LOGIQ, Single Headset

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility