Caveat Emptor: When you are reviewing our testimonials displayed on this website. Sometimes the opinions may be from only one person and may not be representative of all clients, clinicians, customers or users at all times.
The information at this website including the science pages, doctor’s letters and the testimonials from our customers are not meant to imply that you will receive similar or identical results. It is very important that you do independent research before ordering a Curatron 2000 product. The information provided in this website is not medical advice.
Readers are encouraged to obtain the help, services, and recommendations of doctors and other licensed medical practitioners. The webmaster and none of us at Amjo Corp are not medically trained and we are selling this product as a business and for profit. In the USA, the Curatron 2000 series have not yet been granted FDA approval as a medical device.
In Canada, the Curatron product has been licensed by Health Canada as a Class 2 Medical Device. Please read and heed all the information provided by your doctor and in the manual provided with the products we sell. We strive for accuracy. It’s possible that there are errors on this website, you the web visitor should take the time to perform thorough research independently of this web site, Amjo Corp and Curatronic Ltd. cannot be your sole source of information.
We encourage you to do independent research of this technology. Please do not use this website as your sole source of information for PEMF Technology. Outside the USA pulsed magnetic field therapy (PEMF) has been approved in some countries, 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 Curatron 2000 has been approved and registered with Health Canada. See Health Canada Approves the Curatron/ The devices are manufactured according to ISO 13485 for Good Manufacturing Practice.
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