BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Integra Dermal Regeneration Template Single Layer Thin

    Reg #: 2648988 · FEI: 3000204775 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    INTEGRA NEUROSCIENCES
    Registration Number
    2648988
    FEI Number
    3000204775
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    ROAD 402 NORTH, KM 1.2
    City
    ANASCO
    State
    PR
    ZIP
    00610
    Country
    US

    Owner / Operator

    Firm Name
    Integra LifeSciences Corporation
    Operator Number
    9004007
    Address
    1100 Campus Rd
    City
    Princeton
    State
    NJ
    Postal Code
    08540
    Country
    US

    Products

    Device Name Product Code
    Device, Dermal Replacement MDD

    Proprietary Names

    Integra Dermal Regeneration Template Single Layer Thin Integra Dermal Regeneration Template Single Layer Integra Meshed Dermal Regeneration Template (OUS)

    Establishment Types

    Manufacture Device in the United States for Export Only