BEUDAMED
    FDA Registration Active 🇺🇸 United States

    THE REFLUX COMPANY

    Reg #: 3039167637 · FEI: 3039167637 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    9
    Establishment Types
    3
    Classifications
    4

    Registration Details

    Registration Name
    THE REFLUX COMPANY
    Registration Number
    3039167637
    FEI Number
    3039167637
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    7868 Silverton Ave Ste J
    City
    San Diego
    State
    CA
    ZIP
    92126
    Country
    US

    Regulatory Submissions

    510(k) Number
    K173934

    Owner / Operator

    Firm Name
    The Reflux Company
    Operator Number
    10093713
    Address
    7868 Silverton Avenue, Suite J
    City
    San Diego
    State
    CA
    Postal Code
    92126
    Country
    US
    Correspondent
    Thomas Ball

    Products

    Device Name Product Code
    External Upper Esophageal Sphincter (Ues) Compression Device PKA
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Transducer, Miniature Pressure IKE
    Electrode, Ph, Stomach FFT

    Proprietary Names

    Reflux Band SECCA Handpiece and Accessory Kit Transducer, Miniature Pressure Dx201 Dx201P Dx-pH Dx201L Stretta MDRF1 Generator

    Establishment Types

    Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device