BEUDAMED
    FDA Registration Active 🇬🇷 Greece

    KFORCE Grip (LBB), KFORCE Muscle Controller (LBB), KFORCE Link (LBB), KFORCE Sens (KQX), KFORCE Bubble (LBB), KFORCE Pla

    Reg #: 3025591939 · FEI: 3025591939 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    KINVENT HELLAS
    Registration Number
    3025591939
    FEI Number
    3025591939
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    14km Thessaloniki, Neon Moudanion, plot 1490
    City
    Thermi Kentriki Makedonia
    Country
    GR

    Owner / Operator

    Firm Name
    KINVENT Hellas
    Operator Number
    10086801
    Address
    14km Thessaloniki, Neon Moudanion, plot 1490
    City
    Thermi
    State
    Kentriki Makedonia
    Postal Code
    57001
    Country
    GR
    Correspondent
    Emmanouil ATHANASOPOULOS

    US Agent

    Business Name
    FDA Listing Inc.
    Contact Name
    Mohsen Aminipour
    Address
    348 4th ave STE 1014
    City
    Brooklyn
    State
    NY
    ZIP
    11215
    Country
    US
    Email
    [email protected]
    Phone
    646 5124798

    Products

    Device Name Product Code
    Dynamometer, Ac-Powered LBB

    Proprietary Names

    KFORCE Grip (LBB), KFORCE Muscle Controller (LBB), KFORCE Link (LBB), KFORCE Sens (KQX), KFORCE Bubble (LBB), KFORCE Pla K-Grip (KFORCE Grip), K-Push (KFORCE Muscle Controller), K-Pull (KFORCE Link), K-Move (KFORCE Sens), K-Bubble (KFORCE Bu

    Establishment Types

    Remanufacture Medical Device Manufacture Medical Device