At iTOVi, our products are truly unique and innovative, and there is tremendous excitement about the results that distributors and consumers experience with our products. It is important to remember, however, that marketing claims not in harmony with applicable laws could jeopardize your ability to continue to successfully market these innovative products.
The iTOVi Scanner is a Class II Exempt Medical Device, does not require 510K Pre-Market submission, and therefore, has not been evaluated by the FDA. Individual iTOVi scan results are not an indication of health condition, and are not intended to diagnose, treat, cure, or prevent any disease. Claims that iTOVi is approved by the FDA or any other government agency are false and strictly prohibited.
If you have any questions about your health, the health of others, if the iTOVi is safe to use, or the products on the iTOVi report, consult your doctor or healthcare provider.