BEUDAMED
    FDA Registration Active 🇺🇸 United States

    GLENOSPHERE TRIAL EXPANDED (36mm & 40mm)

    Reg #: 3009882462 · FEI: 3009882462 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PERRYMAN COMPANY
    Registration Number
    3009882462
    FEI Number
    3009882462
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    149 S Johnson Rd
    City
    Houston
    State
    PA
    ZIP
    15342
    Country
    US

    Regulatory Submissions

    510(k) Number
    K180632

    Owner / Operator

    Firm Name
    Perryman Company
    Operator Number
    10042198
    Address
    149 South Johnson Rd
    City
    Houston
    State
    PA
    Postal Code
    15342
    Country
    US
    Correspondent
    Dylan Crawford

    Products

    Device Name Product Code
    Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented KWS

    Proprietary Names

    GLENOSPHERE TRIAL EXPANDED (36mm & 40mm) GLENOSPHERE TRIAL (36mm & 40mm)

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)