BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Sixarp LLC, Praxis

    Reg #: 1000115322 · FEI: 1000115322 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Sixarp LLC, Praxis
    Registration Number
    1000115322
    FEI Number
    1000115322
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7650 Caterpillar Ct SW Ste D
    City
    Grand Rapids
    State
    MI
    ZIP
    49548
    Country
    US

    Owner / Operator

    Firm Name
    Sixarp LLC, Praxis
    Operator Number
    10031872
    Address
    7650 Caterpillar Dr, Suite D
    City
    Grand Rapids
    State
    MI
    Postal Code
    49548
    Country
    US
    Correspondent
    John Lowry

    Products

    Device Name Product Code
    Pad, Alcohol, Device Disinfectant LKB

    Establishment Types

    Repack or Relabel Medical Device