BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    Lasik Shield

    Reg #: 3008812251 · FEI: 3002808293 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    11
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Swann-Morton(Services) Limited
    Registration Number
    3008812251
    FEI Number
    3002808293
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Penn Works
    City
    Owlerton Green Sheffield
    Country
    GB

    Regulatory Submissions

    510(k) Number
    K130117

    Owner / Operator

    Firm Name
    SWANN MORTON, LTD.
    Operator Number
    9003320
    Address
    OWLERTON GREEN, --
    City
    SHEFFIELD
    State
    GB-NOTA
    Postal Code
    --
    Country
    GB

    US Agent

    Business Name
    REGULATORY INSIGHT, INC.
    Contact Name
    KEVIN WALLS
    Address
    33 Golden Eagle Lane
    City
    Littleton
    State
    CO
    ZIP
    80127
    Country
    US
    Email
    [email protected]
    Phone
    720 9625412

    Products

    Device Name Product Code
    Sponge, Ophthalmic HOZ

    Proprietary Names

    Lasik Shield Wick and Wipe Eye Wick PVA Point Lasik Drain PVA Spear Eye Shield Instrument Wipe Eye Drain Cellulose Point Cellulose Spear

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)