BEUDAMED
    FDA Registration Active 🇺🇸 United States

    WELLlife™ COVID-19 / Flu A&B Home Test

    Reg #: 3016252795 · FEI: 3016252795 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Wondfo USA Co., Ltd.
    Registration Number
    3016252795
    FEI Number
    3016252795
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    6720 Cobra Way
    City
    San Diego
    State
    CA
    ZIP
    92121
    Country
    US

    Regulatory Submissions

    510(k) Number
    K243256

    Owner / Operator

    Firm Name
    Wondfo USA Co., Ltd.
    Operator Number
    10028951
    Address
    890 REMINGTON BLVD
    City
    Bolingbrook
    State
    IL
    Postal Code
    60440
    Country
    US
    Correspondent
    Kunyuan Mao

    Products

    Device Name Product Code
    Multi-Analyte Respiratory Virus Antigen Detection Test SCA

    Proprietary Names

    WELLlife™ COVID-19 / Flu A&B Home Test INDICAID™ COVID-19 / Flu A&B Home Test WELLlife™ COVID-19 / Influenza A&B Antigen Test

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device