BEUDAMED
    FDA Registration Active 🇨🇭 Switzerland

    MODULITH SLK

    Reg #: 9613347 · FEI: 3002808188 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STORZ MEDICAL AG
    Registration Number
    9613347
    FEI Number
    3002808188
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    LOHSTAMPFESTRASSE 8
    City
    TAEGERWILEN Thurgau
    Country
    CH

    Regulatory Submissions

    510(k) Number
    K010340

    Owner / Operator

    Firm Name
    STORZ MEDICAL AG
    Operator Number
    9028780
    Address
    LOHSTAMPFESTRASSE 8, --
    City
    TAEGERWILEN
    State
    Thurgau
    Postal Code
    CH-8274
    Country
    CH

    US Agent

    Business Name
    STORZ MEDICAL AMERICA INC.
    Contact Name
    Cory Alcala
    Address
    1000 COBB PLACE BLVD., BUILDING 400, SUITE 450
    City
    Kennesaw
    State
    GA
    ZIP
    30144
    Country
    US
    Email
    [email protected]
    Phone
    678 3456229 ext. 8812

    Products

    Device Name Product Code
    Lithotriptor, Extracorporeal Shock-Wave, Urological LNS

    Proprietary Names

    MODULITH SLK

    Establishment Types

    Manufacture Medical Device