BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Smith & Nephew

    Reg #: 3009973505 · FEI: 3009973505 · Expires 2025
    View on FDA
    Products
    13
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    13

    Registration Details

    Registration Name
    ARCH Medical Solutions - Memphis
    Registration Number
    3009973505
    FEI Number
    3009973505
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7580 BARTLETT CORPORATE DR
    City
    BARTLETT
    State
    TN
    ZIP
    38133
    Country
    US

    Regulatory Submissions

    510(k) Number
    K123598

    Owner / Operator

    Firm Name
    Arch Medical Solutions
    Operator Number
    10042635
    Address
    7580 Bartlett Corporate Dr.
    City
    Bartlett
    State
    TN
    Postal Code
    38133
    Country
    US
    Correspondent
    Garry M Smith

    Products

    Device Name Product Code
    Cerclage, Fixation JDQ
    Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented KWY
    Mesh, Surgical, Acetabular, Hip, Prosthesis JDJ
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented JDI
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented LPH
    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented LZO
    Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented LWJ
    Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate MEH
    Prosthesis, Hip, Femoral Component, Cemented, Metal JDG
    Prosthesis, Hip, Hemi-, Femoral, Metal KWL
    Prosthesis, Hip, Hemi-, Femoral, Metal Ball LZY
    Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous MBL
    Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer KWZ

    Proprietary Names

    Smith & Nephew

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)