BEUDAMED
    FDA Registration Active 🇺🇸 United States

    KWIK KLEEN® Kerrisons

    Reg #: 2085947 · FEI: 3000204191 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
    Registration Number
    2085947
    FEI Number
    3000204191
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    22134 SHERMAN WAY
    City
    CANOGA PARK
    State
    CA
    ZIP
    91303
    Country
    US

    Regulatory Submissions

    510(k) Number
    K023868

    Owner / Operator

    Firm Name
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
    Operator Number
    9027397
    Address
    22134 SHERMAN WAY, --
    City
    Canoga Park
    State
    CA
    Postal Code
    91303
    Country
    US
    Correspondent
    JOHN - DAWOODJEE

    Products

    Device Name Product Code
    Rongeur, Manual HAE

    Proprietary Names

    KWIK KLEEN® Kerrisons AED Kerrisons Spine Pro Kerrisons

    Establishment Types

    Repack or Relabel Medical Device