In
1989, INSERM unit U281(French National Institute for Health and Medical
Research), the Urology service of the Edouard Herriot Hospital
Lyon, France and EDAP Technomed joined efforts and initiated
a research project in France. This project was to develop an
efficient and minimally invasive treatment for localized prostate
cancer (stages T1-T2). After ten years of development, the Ablatherm
was CE marked (European approval) and the FDA gave approval
for the United States to conduct a clinical study.
Today thousands of prostate cancer patients
have been treated in several European centers.
The Ablatherm is approved for marketing and
distribution in Europe, Canada, Australia, Russia and South Korea.