BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Digital Fertility Testing System

    Reg #: 3022314446 · FEI: 3022314446 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    FEMOMETER INC
    Registration Number
    3022314446
    FEI Number
    3022314446
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    100 Overlook Center FL 2 Princeton, NJ 08540
    City
    Princeton
    State
    NJ
    ZIP
    08540
    Country
    US

    Owner / Operator

    Firm Name
    Femometer Inc
    Operator Number
    10084923
    Address
    100 Overlook Center FL 2 Princeton, NJ 08540
    City
    Princeton
    State
    NJ
    Postal Code
    08540
    Country
    US
    Correspondent
    Alison Yang

    Products

    Device Name Product Code
    Test, Luteinizing Hormone (Lh), Over The Counter NGE

    Proprietary Names

    Digital Fertility Testing System LH One Step Ovulation Test Midstream,LH One Step Ovulation Test Strip,LH One Step Ovulation Test Cassette femometer FM-IVY-103 with Femometer Period Tracker app femometer Fertility Tracking Kit

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198