BEUDAMED
    FDA Registration Active 🇧🇪 Belgium

    Zimmer Patient Specific Instruments

    Reg #: 3003998208 · FEI: 3003998208 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    MATERIALISE N.V.
    Registration Number
    3003998208
    FEI Number
    3003998208
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    15 TECHNOLOGIELAAN
    City
    LEUVEN Vlaams Brabant
    Country
    BE

    Regulatory Submissions

    510(k) Number
    K111492

    Owner / Operator

    Firm Name
    MATERIALISE N.V.
    Operator Number
    9029485
    Address
    Technologielaan 15, --
    City
    Leuven
    State
    BE-NOTA
    Postal Code
    3001
    Country
    BE

    US Agent

    Business Name
    Materialise USA
    Contact Name
    Jenny Jones
    Address
    44650 Helm Court
    City
    Plymouth
    State
    MI
    ZIP
    48170
    Country
    US
    Email
    [email protected]
    Phone
    734 2597017

    Products

    Device Name Product Code
    Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer MBH
    Knee Arthroplasty Implantation System OOG
    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer JWH

    Proprietary Names

    Zimmer Patient Specific Instruments Zimmer Patient Specific Instruments Planner Zimmer Patient Specific Instruments System

    Establishment Types

    Manufacture Medical Device