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
    K190392

    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
    Powered Laser Surgical Instrument GEX
    Keratome, Ac-Powered HNO

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility