BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ARMM, INC.

    Reg #: 2028523 · FEI: 1000125147 · Expires 2025
    View on FDA
    Products
    4
    Proprietary Names
    0
    Establishment Types
    2
    Classifications
    4

    Registration Details

    Registration Name
    ARMM, INC.
    Registration Number
    2028523
    FEI Number
    1000125147
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    17744 SAMPSON LN.
    City
    HUNTINGTON BEACH
    State
    CA
    ZIP
    92647
    Country
    US

    Regulatory Submissions

    PMA Number
    P990071

    Owner / Operator

    Firm Name
    ARMM, INC.
    Operator Number
    9005125
    Address
    17744 SAMPSON LN., --
    City
    Huntington Beach
    State
    CA
    Postal Code
    92647
    Country
    US
    Correspondent
    ROGER - WOOD

    Products

    Device Name Product Code
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE
    Catheter, Electrode Recording, Or Probe, Electrode Recording DRF
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter OAD
    Cardiac Ablation Percutaneous Catheter LPB

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Sterilize Medical Device for Another Party (Contract Sterilizer)