BEUDAMED
    FDA Registration Active 🇺🇸 United States

    STERISIL ANTIMICROBIAL TUBING AND BOTTLE

    Reg #: 3005844469 · FEI: 3005844469 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Sterisil
    Registration Number
    3005844469
    FEI Number
    3005844469
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4220 Mark Dabling Blvd
    City
    Colorado Spgs
    State
    CO
    ZIP
    80907
    Country
    US

    Regulatory Submissions

    510(k) Number
    K031681

    Owner / Operator

    Firm Name
    Solmetex (Sterisil)
    Operator Number
    9090239
    Address
    4220 Mark Dabling Blvd
    City
    Colorado Springs
    State
    CO
    Postal Code
    80907
    Country
    US
    Correspondent
    Curtis D Conley

    Products

    Device Name Product Code
    Unit, Operative Dental EIA

    Proprietary Names

    STERISIL ANTIMICROBIAL TUBING AND BOTTLE

    Establishment Types

    Repack or Relabel Medical Device Manufacture Medical Device