BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    KEELER LTD.

    Reg #: 1000391004 · FEI: 1000391004 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    KEELER LTD.
    Registration Number
    1000391004
    FEI Number
    1000391004
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    CLEWER HILL RD.
    City
    WINDSOR, BERKSHIRE Windsor and Maidenhead
    Country
    GB

    Regulatory Submissions

    510(k) Number
    K942180

    Owner / Operator

    Firm Name
    KEELER LTD.
    Operator Number
    9011500
    Address
    CLEWER HILL RD.
    City
    WINDSOR, BERKSHIRE
    State
    GB-NOTA
    Postal Code
    SL4 4AA
    Country
    GB
    Correspondent
    Claudia B Hill

    US Agent

    Business Name
    Keeler USA
    Contact Name
    Claudia Hill
    Address
    3222 Phoenixville Pike
    City
    Malvern
    State
    PA
    ZIP
    19355
    Country
    US
    Email
    [email protected]
    Phone
    610 8890200

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX
    Laser, Ophthalmic HQF

    Establishment Types

    Manufacture Medical Device