Outside the USA pulsed magnetic 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.
- Readers are encouraged to obtain the help, services and recommendations of doctors and other licensed medical practitioners.Do not use this website as your sole source of information for PEMF Technology.
- In the United States of America the Curatron devices have not been cleared by the FDA for any use. 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. The devices are manufactured according to ISO 13485 for Good Manufacturing Practice.
- In Canada, the Curatron 2000 systems have been approved by Health Canada and have been cleared for use at home and in clinics.