BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ProTech Plus Self Cure Hard Reline and Repair Acrylic

    Reg #: 2435952 · FEI: 1000137415 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PROTECH PROFESSIONAL PRODUCTS, INC.
    Registration Number
    2435952
    FEI Number
    1000137415
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2900 Commerce Park Dr Ste 10
    City
    BOYNTON BEACH
    State
    FL
    ZIP
    33426
    Country
    US

    Regulatory Submissions

    510(k) Number
    K131036

    Owner / Operator

    Firm Name
    PROTECH PROFESSIONAL PRODUCTS, INC.
    Operator Number
    9006187
    Address
    2900 NW COMMERCE PARK DR., #10
    City
    Boynton Beach
    State
    FL
    Postal Code
    33426
    Country
    US
    Correspondent
    RANDI - BLOCH

    Products

    Device Name Product Code
    Resin, Denture, Relining, Repairing, Rebasing EBI

    Proprietary Names

    ProTech Plus Self Cure Hard Reline and Repair Acrylic ProTech UBAR Metal Bonding Acrylic

    Establishment Types

    Repack or Relabel Medical Device