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The company’s devices are FDA-cleared Class II medical devices for temporary relief of minor muscle/joint pain and related symptoms. Over ten thousand units have been sold with more than twenty-five million treatments reported without adverse events. Clinical results emphasize safety and efficacy in noninvasive microcirculation enhancement for chronic pain management. The technology has also received CE Mark approval in the EU for improving whole-body microcirculation—claimed to support wound healing processes such as diabetic foot ulcers.
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