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StemWave Introduces Modus-F, A New FDA Listed Device With Cellular Response Therapy (CRT) Now Available For Orthopedic Use

March 28, 2022 – StemWave recently announced that their newest device Modus-F is now available for sale. StemWave recently received a Class l listing from the FDA and announced an exclusive North American partnership with Inceler Medikal, a leading global manufacturer.

StemWave’s newest product, Modus-F, uses uniquely designed Cellular Response Therapy (CRT) which utilizes an electrohydraulic system that generates focused acoustic waves that apply mechanical force and energy to living tissue.

StemWave will offer Modus-F to orthopedic healthcare providers like physical therapists, chiropractors, medical spas, and more.

Read more: https://www.digitaljournal.com/pr/stemwave-introduces-modus-f-a-new-fda-listed-device-with-area-directed-technology-adt-now-available-for-orthopedic-use#ixzz8HwIFJQMc

 

 

Intended Use Modus-F by StemWave: The Modus-F by StemWave, utilizing Cellular Response Technology, is intended for use in addressing minor aches and pains in accordance with the User Manual (IFU). Use of the product for any other purpose has not been reviewed by the U.S. Food and Drug Administration and is considered off-label use. Please consult the User Manual (IFU) and all labeling provided with the product prior to use.

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Individual results may vary. Neither StemWave nor any of its subsidiaries dispense medical advice. The contents of this website do not constitute medical, legal, or any other type of professional advice. Information related to various health, medical, and fitness conditions and their treatment is not meant to be a substitute for the advice provided by a physician or other medical professional. You should not use the information contained herein for diagnosing a health or fitness problem or disease. Rather, please consult your healthcare professional for information on the courses of treatment, if any, which may be appropriate for you.

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