Vishee Medical Announces Second-Generation Mental Health Magnetic Stimulation Device to Enter FDA Filing Process in Second Half of 2023

VISHEE Medical recently stated in a research report that the company's Body Shaping Magnetic product completed FDA 510(k) registration and obtained certification in March this year. The process for obtaining medical registration certification in China is currently proceeding actively. The second-generation pelvic floor magnetic product has now initiated FDA registration, and the second-generation mental health magnetic product is expected to start the FDA registration process in the second half of this year.