BEUDAMED
    FDA Registration Active 🇰🇷 South Korea

    FEELject LDV(Low dead volume) Syringe

    Reg #: 3010462274 · FEI: 3010462274 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    FEELTECH CO.,LTD.
    Registration Number
    3010462274
    FEI Number
    3010462274
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4 Floor, Standard Factory 5-dong, part of 1 Floor, Standard Factory 1-dong, part of 3, 4 Floor, Standard Factory 2-dong,15, Jayumuyeok 2-gil
    City
    Gunsan-si Jeonbuk
    Country
    KR

    Regulatory Submissions

    510(k) Number
    K213010

    Owner / Operator

    Firm Name
    Feeltech Co.,Ltd.
    Operator Number
    10050336
    Address
    4th Floor, Standard Factory5-dong, 1st Floor, Standard Factory1-dong, 3rd- 4th Floors, Standard Factory2-dong, 15, Jayumuyeok 2-gil
    City
    Gunsan-si
    State
    Jeonbuk
    Postal Code
    54001
    Country
    KR
    Correspondent
    Geun Sik Kim

    US Agent

    Business Name
    Kelly Medical Consulting
    Contact Name
    Kelly Kim
    Address
    2700l La Paz Road, Suite 314
    City
    Mission Viejo
    State
    CA
    ZIP
    92691
    Country
    US
    Email
    [email protected]
    Phone
    949 2937124

    Products

    Device Name Product Code
    Low Dead Space Piston Syringe QNQ
    Needle, Hypodermic, Single Lumen FMI

    Proprietary Names

    FEELject LDV(Low dead volume) Syringe

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device