Disclaimer: pulsed electromagnetic field therapy (PEMF) has been approved by health authorities as medical therapy for human applications. In the European Community the Curatron devices are certified as medical devices according to the medical device directive 93/42/EEC. The devices are manufactured according to ISO 13485 for good manufacturing practice. In Canada the Curatron devices are now licensed by Health Canada. In the united states of America, the Curatron devices have not been cleared by the FDA. The information provided on this website is not medical advice. The products marketed on this website are not intended to diagnose, treat, cure or prevent any disease. Readers are encouraged to obtain the help, services and recommendations of doctors and other licensed medical practitioners.