BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Lief Device Facility

    Reg #: 3015542403 · FEI: 3015542403 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

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    Registration Details

    Registration Name
    Lief Device Facility
    Registration Number
    3015542403
    FEI Number
    3015542403
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    2703 7th Street, Suite #301, Mailbox #123
    City
    Berkeley
    State
    CA
    ZIP
    94710
    Country
    US

    Owner / Operator

    Firm Name
    Zenso, Inc.
    Operator Number
    10060541
    Address
    2443 Fillmore St #380-6060
    City
    San Francisco
    State
    CA
    Postal Code
    94115
    Country
    US
    Correspondent
    William Frese

    Products

    Device Name Product Code
    Device, Biofeedback HCC

    Proprietary Names

    Lief Rx

    Establishment Types

    Manufacture Medical Device