BEUDAMED
    FDA Registration Active 🇺🇸 United States

    CORVITEX CORPORATION

    Reg #: 3039062605 · FEI: 3039062605 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

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    Registration Details

    Registration Name
    CORVITEX CORPORATION
    Registration Number
    3039062605
    FEI Number
    3039062605
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    4928 Windy Hill Dr Ste B
    City
    Raleigh
    State
    NC
    ZIP
    27609
    Country
    US

    Regulatory Submissions

    510(k) Number
    K250972

    Owner / Operator

    Firm Name
    Corvitex Corporation
    Operator Number
    10092281
    Address
    4928 B Windy Hill Drive
    City
    Raleigh
    State
    NC
    Postal Code
    27609
    Country
    US
    Correspondent
    Bettina Nolan

    Products

    Device Name Product Code
    Catheter, Percutaneous DQY

    Proprietary Names

    Primum Guiding Catheter

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198