Femasys Receives AMA CPT Editorial Panel Approval for New Category III CPT Code for FemaSeed Intratubal Insemination

Core Insights - Femasys Inc. has received approval from the American Medical Association (AMA) for a new Category III CPT code for its FemaSeed intratubal insemination (ITI) procedure, which is set to take effect on January 1, 2027, enhancing reimbursement strategies and patient access to this infertility treatment [1][2] Company Overview - Femasys is a biomedical innovator focused on making fertility and non-surgical permanent birth control more accessible and cost-effective for women globally, with a patent-protected portfolio of therapeutic and diagnostic products [3] - The company's fertility portfolio includes FemaSeed ITI, FemSperm, and FemVue, with FemaSeed demonstrating more than double the pregnancy rates of traditional intrauterine insemination (IUI) in clinical trials [3] Product Details - FemaSeed is designed to improve fertilization by delivering sperm directly to the fallopian tube, offering a less invasive and more cost-effective alternative to traditional IUI and in vitro fertilization (IVF) [2] - FemBloc, another product, is the first non-surgical, in-office alternative to surgical sterilization, receiving regulatory approval in Europe, the UK, and New Zealand in 2025 [4] Market Strategy - The approval of the CPT code is expected to support broader clinical adoption and provider utilization of FemaSeed, aiming to reach over 10 million women in the U.S. affected by infertility [2] - Femasys plans to expand its provider footprint and accelerate adoption through the rollout of FemaSeed and the availability of its FemSperm product line [2]