BEUDAMED
    FDA Registration Active 🇺🇸 United States

    0792-002, 12-14F Dilator

    Reg #: 1722746 · FEI: 1000306216 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    MEDRON, LLC
    Registration Number
    1722746
    FEI Number
    1000306216
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1518 S Gladiola St
    City
    SALT LAKE CITY
    State
    UT
    ZIP
    84104
    Country
    US

    Regulatory Submissions

    510(k) Number
    K971897

    Owner / Operator

    Firm Name
    MEDRON, LLC
    Operator Number
    9010139
    Address
    1518 SOUTH GLADIOLA ST., --
    City
    Salt Lake City
    State
    UT
    Postal Code
    84104
    Country
    US
    Correspondent
    Sommer Altvater

    Products

    Device Name Product Code
    Dilator, Vessel FKA
    Catheter, Femoral LFK

    Proprietary Names

    0792-002, 12-14F Dilator

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device