BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Canady Hybrid Plasma Scalpel

    Reg #: 3008849319 · FEI: 3008849319 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    Canady Biotechnology LLC
    Registration Number
    3008849319
    FEI Number
    3008849319
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6930 Carroll Ave
    City
    Takoma Park
    State
    MD
    ZIP
    20912
    Country
    US

    Regulatory Submissions

    510(k) Number
    K113500

    Owner / Operator

    Firm Name
    US Medical Innovations
    Operator Number
    10047595
    Address
    6930 Carroll Avenue, 10th Floor, Suite 1000
    City
    Takoma Park
    State
    MD
    Postal Code
    20912
    Country
    US
    Correspondent
    Katherine Korinko

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI

    Proprietary Names

    Canady Hybrid Plasma Scalpel Canady Viera Hybrid Plasma Scapel

    Establishment Types

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