PEMF FLASH System Intensity
Pain vs Pain
Curatron FLASH and other Impulse systems typically provide virtual immediate pain relief and the Curatron FLASH system is no exception. Impulse systems can also introduce pain and discomfort during treatment as their individual impulses can be extremely high and these impulses cause our nerves to react and our muscles to twitch, contract, and spasm. The higher the intensity, the greater the twitch or muscle contraction.
While you are looking at the comparisons below. Remember that the FLASH has 10 built-in programs to the competitor’s three or so. The FLASH has available software (optional) to allow you to create and store protocols and patient data. The FLASH also has an optional 18″x23″ pad for larger area treatment.
Curatron FLASH Intensities
- 3500 Gauss – Competitor’s Impulse System (Fully Electronic) The FLASH is Fully Electronic TOO
- 4000 Gauss – Curatron FLASH with Standard Applicator (12″ Loop)
- 4000 Gauss Curatron FLASH with Optional 18″x23″ Mat (Booster Off)
- 5400 Gauss Curatron FLASH with Booster and Standard Coil Applicator
- 5400 Gauss Curatron FLASH with Optional 18″x23″ Mat (Booster On)
- 5400 Gauss Curatron FLASH with 7×7 Pad (Booster Off)
- 7000 Gauss Curatron FLASH with 7×7 Pad (Booster On)
Yes the FLASH has a lower intensity than the MG33, PEMF120, PEMF100, and the PulseCenter machines BUT SO WHAT!
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.