BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    WAVELIGHT GmbH

    Reg #: 9710340 · FEI: 3002483854 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    0
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    WAVELIGHT GmbH
    Registration Number
    9710340
    FEI Number
    3002483854
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    AM WOLFSMANTEL 5
    City
    ERLANGEN Bavaria
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K101006

    Owner / Operator

    Firm Name
    Alcon Laboratories, Inc.
    Operator Number
    1610287
    Address
    6201 SOUTH FREEWAY
    City
    Fort Worth
    State
    TX
    Postal Code
    76134
    Country
    US

    Products

    Device Name Product Code
    Keratome, Ac-Powered HNO
    Powered Laser Surgical Instrument GEX

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility