BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Light pad and Light probe

    Reg #: 3013069546 · FEI: 3013069546 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ASCENTRON, INC.
    Registration Number
    3013069546
    FEI Number
    3013069546
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    994 Antelope Rd.
    City
    White City
    State
    OR
    ZIP
    97503
    Country
    US

    Regulatory Submissions

    510(k) Number
    K113250

    Owner / Operator

    Firm Name
    Ascentron, Inc.
    Operator Number
    10060122
    Address
    994 Antelope Rd.
    City
    White City
    State
    OR
    Postal Code
    97503
    Country
    US
    Correspondent
    Amanda Brewer

    Products

    Device Name Product Code
    Lamp, Infrared, Therapeutic Heating ILY

    Proprietary Names

    Light pad and Light probe

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)