BEUDAMED
    FDA Registration Active 🇰🇷 South Korea

    Neo Anchor plus

    Reg #: 3008959419 · FEI: 3008959419 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    KJ MEDITECH CO., LTD.
    Registration Number
    3008959419
    FEI Number
    3008959419
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    21, Cheomdan venture-ro, 40 beon-gil, Buk-gu
    City
    Gwangju
    Country
    KR

    Regulatory Submissions

    510(k) Number
    K053629

    Owner / Operator

    Firm Name
    KJ Meditech Co., Ltd.
    Operator Number
    10035757
    Address
    21, Cheomdan venture-ro, 40 beon-gil, Buk-gu
    City
    Gwangju
    State
    KR-NOTA
    Postal Code
    61009
    Country
    KR
    Correspondent
    Hyukki Moon

    US Agent

    Business Name
    LK Consulting Group USA, Inc.
    Contact Name
    Priscilla Chung
    Address
    18881 Von Karman Ave STE 160
    City
    Irvine
    State
    CA
    ZIP
    92612
    Country
    US
    Email
    [email protected]
    Phone
    714 2025789

    Products

    Device Name Product Code
    Implant, Endosseous, Root-Form DZE

    Proprietary Names

    Neo Anchor plus Anchor plus

    Establishment Types

    Manufacture Medical Device