BEUDAMED
    FDA Registration Active 🇺🇸 United States

    LACRIFILL® Canalicular Gel

    Reg #: 3011965331 · FEI: 3011965331 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Nordic Pharma, Inc.
    Registration Number
    3011965331
    FEI Number
    3011965331
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1205 Westlakes Drive, Suite 275
    City
    Berwyn
    State
    PA
    ZIP
    19312
    Country
    US

    Regulatory Submissions

    510(k) Number
    K222164

    Owner / Operator

    Firm Name
    Amring Pharmaceuticals Inc.
    Operator Number
    10056388
    Address
    1205 Westlakes Drive, Suite 275
    City
    Berwyn
    State
    PA
    Postal Code
    19312
    Country
    US
    Correspondent
    Melissa Goodhead

    Products

    Device Name Product Code
    Plug, Punctum LZU

    Proprietary Names

    LACRIFILL® Canalicular Gel

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility