BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Canady Biotechnology LLC

    Reg #: 3008849319 · FEI: 3008849319 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    13
    Establishment Types
    4
    Classifications
    2

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    Registration Details

    Registration Name
    Canady Biotechnology LLC
    Registration Number
    3008849319
    FEI Number
    3008849319
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    6930 Carroll Ave
    City
    Takoma Park
    State
    MD
    ZIP
    20912
    Country
    US

    Regulatory Submissions

    510(k) Number
    K240297

    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
    Low Energy Direct Current Thermal Ablation System OAB

    Proprietary Names

    Canady Helios Cold Plasma XL-1000CP Ablation System Canady Hybrid Plasma Scalpel Canady Viera Hybrid Plasma Scapel Canady Plasma Electrosurgical Unit & Accessories Canady Plasma Electrosurgical Unit Series SS601MCA, SS-200E/Canady Plasma Coagulator Argon 2 and Argon 4 with acccess. Canady Plasma Electrosurgical Unit Series SS601MCA, SS-200E/Canady Plasm Coagulator Argon 2 and Argon 4 with accessories Canady Viera Hybrid Plasma Scalpel Canady Argon Plasma Probes Canady Plasma TBS Probe Canady Plasma Probes for Flexible Endoscopy Canady Plasma GIT Probe Canady Plasma SMART XL-1000 Electrosurgical Generator with Accessories Canady Argon Plasma Probe

    Establishment Types

    Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility