BEUDAMED
    FDA Registration Active 🇫🇷 France

    K-Move

    Reg #: 3016566173 · FEI: 3016566173 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    17
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    KINVENT BIOMECANIQUE
    Registration Number
    3016566173
    FEI Number
    3016566173
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6 Rue de Pommessargues
    City
    Montepellier Herault
    Country
    FR

    Owner / Operator

    Firm Name
    Kinvent Biomecanique SAS
    Operator Number
    10062556
    Address
    6 Rue de Pommessargues
    City
    Montepellier
    State
    Herault
    Postal Code
    34000
    Country
    FR
    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
    Device, Biofeedback HCC

    Proprietary Names

    K-Move K-Force K-FORCE K Myo Black K-LAB K-Pull K-Deltas K-Bubble K Myo KFORCE KMYO K-Myo K-Deltas XL K-Grip KINVENT K-Force Plates K-Push

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device