BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CPM PAD KIT, KINETIC 7080 SHOULDER, KT-78

    Reg #: 2031918 · FEI: 3002935344 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    13
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    TIBURON MEDICAL ENTERPRISES
    Registration Number
    2031918
    FEI Number
    3002935344
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    915 INDUSTRIAL WAY
    City
    SAN JACINTO
    State
    CA
    ZIP
    92582
    Country
    US

    Owner / Operator

    Firm Name
    TIBURON MEDICAL ENTERPRISES
    Operator Number
    9040187
    Address
    915 INDUSTRIAL WAY, --
    City
    San Jacinto
    State
    CA
    Postal Code
    92582
    Country
    US

    Products

    Device Name Product Code
    Components, Exercise IOD

    Proprietary Names

    CPM PAD KIT, KINETIC 7080 SHOULDER, KT-78 CPM PAD KIT, ARTROMOT PRO SHOULDER WITHOUT SEAT PAD 5624-86 Liner Only, Portable Hand CPM Bilateral Splint 5624-83 Bilateral Portable Hand CPM Splint-Universal 5624-84 Aluma Foam Component only-Port Hand CPM Bilateral Splint CPM Pad Kit Knab 450, #9501-10 CPM Pad Kit, Danninger 500 Series Knee, DA-50E NC92063 Optiflex Knee CPM Kit 5624-85 Straps & Pads Only, Portable Hand CPM Bilateral Splint CPM W2-101 SG Patient Kit RevD CPM Pad Kit, Danninger 400 Series Knee, Universal CPM PAD KIT, KINETIC CENTURA SHOULDER, KT-CT CPM PAD KIT, ARTROMOT PRO SHOULDER, AR-MT - AR2

    Establishment Types

    Manufacture Medical Device