BEUDAMED
    FDA Registration Active 🇺🇸 United States

    SMF

    Reg #: 3007366790 · FEI: 3007282753 · Expires 2025
    View on FDA
    Products
    13
    Proprietary Names
    14
    Establishment Types
    1
    Classifications
    13

    Registration Details

    Registration Name
    Smith & Nephew, Inc.
    Registration Number
    3007366790
    FEI Number
    3007282753
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    3303 E Holmes Rd
    City
    Memphis
    State
    TN
    ZIP
    38118
    Country
    US

    Regulatory Submissions

    510(k) Number
    K123598

    Owner / Operator

    Firm Name
    Smith & Nephew, Inc.
    Operator Number
    1020279
    Address
    2875 Railroad Street
    City
    Pittsburgh
    State
    PA
    Postal Code
    15222
    Country
    US
    Correspondent
    Lisa Ewing

    Products

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

    Proprietary Names

    SMF REFLECTION CONTOUR ECHELON EMPERION CPCS SL PLUS R3 ANTHOLOGY SYNERGY MIA ACCORD SPECTRON MDF

    Establishment Types

    Manufacture Medical Device