BEUDAMED
    FDA Registration Active 🇺🇸 United States

    ARTIA Reconstructive Tissue Matrix Perforated

    Reg #: 1647098 · FEI: 1000306051 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    LIFECELL CORP.
    Registration Number
    1647098
    FEI Number
    1000306051
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    ONE MILLENNIUM WAY
    City
    BRANCHBURG
    State
    NJ
    ZIP
    08876
    Country
    US

    Regulatory Submissions

    510(k) Number
    K162752

    Owner / Operator

    Firm Name
    AbbVie, Inc.
    Operator Number
    2011068
    Address
    2525 DUPONT DRIVE, --
    City
    Irvine
    State
    CA
    Postal Code
    92612
    Country
    US
    Correspondent
    James P Wabby

    Products

    Device Name Product Code
    Mesh, Surgical FTM
    Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery OXH

    Proprietary Names

    ARTIA Reconstructive Tissue Matrix Perforated

    Establishment Types

    Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198