BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Tendon Shuttling Instrument Procedure Pack

    Reg #: 3007593722 · FEI: 3007593722 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    MEDSHAPE, INC.
    Registration Number
    3007593722
    FEI Number
    3007593722
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1575 NORTHSIDE DR NW STE 440
    City
    Atlanta
    State
    GA
    ZIP
    30318
    Country
    US

    Owner / Operator

    Firm Name
    MedShape, Incorporated
    Operator Number
    10026693
    Address
    1575 Northside Drive NW STE 440
    City
    Atlanta
    State
    GA
    Postal Code
    30318
    Country
    US

    Products

    Device Name Product Code
    Kit, Surgical Instrument, Disposable KDD

    Proprietary Names

    Tendon Shuttling Instrument Procedure Pack Transtibial Anterior Cruciate Ligament Kit Tenodesis Accessory Instrument Procedure Pack Disposable Drill and Drill Guide Procedure Pack

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility