BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Aptis

    Reg #: 3003387384 · FEI: 3003387384 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Phillips Precision Inc
    Registration Number
    3003387384
    FEI Number
    3003387384
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    7 Paul Kohner Pl
    City
    Elmwood Park
    State
    NJ
    ZIP
    07407
    Country
    US

    Regulatory Submissions

    510(k) Number
    K082839

    Owner / Operator

    Firm Name
    Phillips Precision Inc/Creighton
    Operator Number
    10042522
    Address
    7 Paul Kohner Place
    City
    Elmwood Park
    State
    NJ
    Postal Code
    07407
    Country
    US
    Correspondent
    Shalyn Creighton

    Products

    Device Name Product Code
    Prosthesis, Wrist, Hemi-, Ulnar KXE

    Proprietary Names

    Aptis

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)