BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LUXCREO INC.

    Reg #: 3016237718 · FEI: 3016237718 · Expires 2026
    View on FDA
    Products
    6
    Proprietary Names
    5
    Establishment Types
    2
    Classifications
    6

    Registration Details

    Registration Name
    LUXCREO INC.
    Registration Number
    3016237718
    FEI Number
    3016237718
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    350 W. Ontario Street Suite 700 Chicago,lL.60654
    City
    Chicago
    State
    IL
    ZIP
    60654
    Country
    US

    Regulatory Submissions

    510(k) Number
    K250343

    Owner / Operator

    Firm Name
    LuxCreo Inc.
    Operator Number
    10071055
    Address
    350 W Ontario Street Suite700Chicago,lL.60654
    City
    Chicago
    State
    IL
    Postal Code
    60654
    Country
    US
    Correspondent
    Tao Feng

    Products

    Device Name Product Code
    Plate, Base, Shellac EEA
    Aligner, Sequential NXC
    Maintainer, Space Preformed, Orthodontic DYT
    Positioner, Tooth, Preformed KMY
    Mouthguard, Prescription MQC
    Resin, Denture, Relining, Repairing, Rebasing EBI

    Proprietary Names

    LuxCreo Dental Night Guard Resin LuxCreo Clear Aligner System LuxCreo Dental Clear Aligner Resin LuxCreo Clear Retainer System FPD Reisn

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device