BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CDR Manufacturing, Inc., DBA Keytronic

    Reg #: 3003857828 · FEI: 3003857828 · Expires 2026
    View on FDA
    Products
    8
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    7

    Registration Details

    Registration Name
    CDR Manufacturing, Inc., DBA Keytronic
    Registration Number
    3003857828
    FEI Number
    3003857828
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    7015 55TH ST N
    City
    Oakdale
    State
    MN
    ZIP
    55128
    Country
    US

    Owner / Operator

    Firm Name
    Key Tronic
    Operator Number
    10050703
    Address
    4424 N Sullivan Rd
    City
    Spokane Valley
    State
    WA
    Postal Code
    99216
    Country
    US

    Products

    Device Name Product Code
    System, Thermal Regulating DWJ
    LOS
    Monitor, St Segment With Alarm MLD
    Electrocardiograph DPS
    Stimulator, Hypoglossal Nerve, Implanted, Apnea MNQ
    System, Imaging, Pulsed Echo, Ultrasonic IYO
    Plethysmograph, Impedance DSB
    Monitor, Extracellular Fluid, Lymphedema, Extremity OBH

    Proprietary Names

    Pintler Patient Warming System Vectraplexecg system with vectraplexami Universal SmartECG INSPIRE II UPPER AIRWAY STIMULATOR VitaScan LT SOZO

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)