BEUDAMED
    FDA Registration Active 🇺🇸 United States

    SMF

    Reg #: 3010886696 · FEI: 3010886696 · Expires 2025
    View on FDA
    Products
    13
    Proprietary Names
    14
    Establishment Types
    1
    Classifications
    13

    Registration Details

    Registration Name
    Smith & Nephew, Inc.
    Registration Number
    3010886696
    FEI Number
    3010886696
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3510 Winchester 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