BEUDAMED
    FDA Registration Active 🇨🇳 China

    NaviCam Xpress Stomach Capsule Endoscope System(NaviCam Xpress Stomach System)

    Reg #: 3017400296 · FEI: 3017400296 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ANKON TECHNOLOGIES CO., LTD.
    Registration Number
    3017400296
    FEI Number
    3017400296
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    No. 666, Hi-tech Road, East Lake New Technology Development Zone
    City
    Wuhan Hubei
    Country
    CN

    Regulatory Submissions

    510(k) Number
    K203192

    Owner / Operator

    Firm Name
    Ankon Technologies Co., Ltd.
    Operator Number
    10077962
    Address
    6010 W Spring Creek Parkway
    City
    Plano
    State
    TX
    Postal Code
    75024
    Country
    US

    Products

    Device Name Product Code
    Magnetically Maneuvered Capsule Endoscopy System QKZ

    Proprietary Names

    NaviCam Xpress Stomach Capsule Endoscope System(NaviCam Xpress Stomach System)

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)