BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Kit, Acteon Curing Lt, S4 Std, White

    Reg #: 3029780 · FEI: 1000523896 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    DCI International, LLC
    Registration Number
    3029780
    FEI Number
    1000523896
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    705 S SPRINGBROOK RD., Bldg C
    City
    NEWBERG
    State
    OR
    ZIP
    97132
    Country
    US

    Regulatory Submissions

    510(k) Number
    K072181

    Owner / Operator

    Firm Name
    DCI International LLC
    Operator Number
    9099996
    Address
    705 S Springbrook Rd, Bldg. C
    City
    Newberg
    State
    OR
    Postal Code
    97132
    Country
    US
    Correspondent
    Dana Shusterman

    Products

    Device Name Product Code
    Activator, Ultraviolet, For Polymerization EBZ

    Proprietary Names

    Kit, Acteon Curing Lt, S4 Std, White Kit, Acteon Curing Lt, Cart Kit, Acteon Curing Lt, S5 Std Curing Light, Mini LED, Acteon Kit, Acteon Curing Lt, S5 Kit, Acteon Curing Lt, S4 Std, Light Gray Kit, Acteon Curing Lt, S4, Light Gray Kit, Acteon Curing Lt, S4, White

    Establishment Types

    Repack or Relabel Medical Device