TWO BASIC TECHNOLOGIES – BOTH CALLED PEMF
Confusion Reigns! What the heck is PEMF anyway? What are the different kinds of PEMF? the choice may not be obvious at first so let me try and guide you to an optimal solution for you. It may not be the only solution but for you, however, it may be the best choice. Let’s look at who you are and your needs?
First! IMPULSE OR REAL PEMF
First of all, let’s look at IMPULSE vs REAL PEMF. Most home users do not select the IMPULSE or RINGER systems for their use. These systems do provide very quick pain relief but do not offer the treatment of the underlying condition(s), so if one is looking heal the problem then the REAL PEMF system (Curatron 2000 Family) is the right choice. If you’re in a clinical environment then the choices become a little blurry.
Are you a home user?
The home user needs a system for his or her personal use and probably does not want the complexity of the additional software that’s available with the Curatron 2000 PC or Curatron 2000 3D. We have sold many PC and 3D systems to home users, but those sales tend to be the exception, not the rule. The two most popular options are the Curatron 2000 HT or the Curatron 2000 XPSE. The HT is less expensive but is more limited as far as options are concerned and roughly one-half of the intensity of the XPSE. If budget is not an issue, then the XPSE is definitely the better choice.
Are you in a clinical environment?
Let’s assume that you have a client who is in pain NOW!
If you need to provide relief NOW then an Impulse System like the FLASH is needed to help reduce the patient’s pain NOW.
Your best options are:
- An Impulse or ringer system such as the FLASH
- The Curatron 2000 3D with its 1600 Gauss Butterfly Coil
- Our LLLT-PEMF Combo Probe (1500 Gauss with 2.3 milli-watts of 640 nm Red Light)
- Note our Combo probe works with the 3D, PC, and XPSE Control Units
Let’s assume that you have a client who needs ongoing treatment.
Remember, the Impulse systems above can and do provide immediate help, but in many cases, they do not treat the underlying issue but only treat the symptoms.
REAL PEMF Systems such as the Curatron 2000 Family treat the underlying condition by reducing inflammation, reducing pain, improving blood flow, etc. etc. Think of the Curatron 2000 Family as the Penicillin while you think of the Impulse Systems as the pain reliever, be it Aspirin or a shot of Novacaine or Lidocaine.
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.