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Question 1
1
Luminance RED products have been registered with the FDA as class II medical devices (ILY). They are manufactured in an FDA-registered facility with ISO 13485 certification in compliance with 21 CFR 820 regulations.
Luminance RED devices are indicated for use in the relief of muscle and joint pain, including arthritis and muscle spasm pain, and increasing blood circulation and relaxation of muscles. They are intended for general medical purposes to provide topical heating. The information provided here is for educational purposes and not a substitute for a face-to-face consultation with your healthcare provider, and should not be construed as medical advice.
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I accept
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B
I don’t accept