BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LAUNCH DEVELOPMENT

    Reg #: 3011657089 · FEI: 3011657089 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    3

    Registration Details

    Registration Name
    LAUNCH DEVELOPMENT
    Registration Number
    3011657089
    FEI Number
    3011657089
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    7791 Aqua Circle, Suite 7G
    City
    Dalton Gardens
    State
    ID
    ZIP
    83815
    Country
    US

    Regulatory Submissions

    510(k) Number
    K140470

    Owner / Operator

    Firm Name
    Launch Development
    Operator Number
    10049473
    Address
    7791 Aqua Circle, Suite 7G
    City
    Dalton Gardens
    State
    ID
    Postal Code
    83815
    Country
    US
    Correspondent
    Anthony Jakubowski

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX
    Dilator, Vessel, For Percutaneous Catheterization DRE
    Introducer, Catheter DYB

    Proprietary Names

    KIT-072-00 CLI-111-00

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility