BEUDAMED
    FDA Registration Active 🇺🇸 United States

    MSK Health Platform

    Reg #: 3023517494 · FEI: 3023517494 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    KINOTEK
    Registration Number
    3023517494
    FEI Number
    3023517494
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    22 Monument Square, Suite 201
    City
    Portland
    State
    ME
    ZIP
    04101
    Country
    US

    Owner / Operator

    Firm Name
    Kinotek
    Operator Number
    10085775
    Address
    22 Monument Square, Suite 201
    City
    Portland
    State
    ME
    Postal Code
    04101
    Country
    US
    Correspondent
    Kaitlyn Haase

    Products

    Device Name Product Code
    Interactive Rehabilitation Exercise Device, Prescription Use QKC

    Proprietary Names

    MSK Health Platform

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device