BEUDAMED
    FDA Registration Active 🇺🇸 United States

    RELIGN CORPORATION

    Reg #: 3012790575 · FEI: 3012790575 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    RELIGN CORPORATION
    Registration Number
    3012790575
    FEI Number
    3012790575
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    1725 De La Cruz Blvd Ste 7
    City
    Santa Clara
    State
    CA
    ZIP
    95050
    Country
    US

    Regulatory Submissions

    510(k) Number
    K162770

    Owner / Operator

    Firm Name
    RELIGN Corporation
    Operator Number
    10053774
    Address
    1725 De La Cruz Blvd Ste 7
    City
    Santa Clara
    State
    CA
    Postal Code
    95050
    Country
    US
    Correspondent
    Michael Duvall

    Products

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

    Proprietary Names

    Relign Arthroscopic System Tricera Tricera™ Arthroscopic System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility