The Curatron Family
Curatronic in Israel is the world’s only manufacturer of both REAL PEMF systems and FLASH or Impulse Systems. Both types of systems are sold and explained at other websites.
- The Curatron FLASH – Impulse/Ringer Systems
- The Curatron 2000 HT (Home Therapy System)
- The Curatron 2000 XP and XPSE (Advanced Home System and Clinical Introductory System)
- The Curatron 2000 PC (PC/MAC Computer Controlled Systems)
- The Curatron 2000 3D Ultra Power (PC/MAC Controlled)
Curatron systems tend to look alike. This is the Curatron FLASH with blue LEDs a blue highlights
There is more to learn!
Amjo Corp has been working with Curatron systems for nearly two decades. Our first sale of a Curatron PEMF system was in May of 2000. Our experience and knowledge are second to none. Call us and find out!
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. 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 devices are manufactured according to ISO 13485 for Good Manufacturing Practice.