Vlight states on their website that their devices are not FDA-approved but are classified as low-risk General Wellness devices under the FDA's draft General Wellness Policy (January 20, 2015) and have been independently TUV-certified as safe for consumer use by a European standard.
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Speaker
Unidentified Speaker — Photobiomodulation Devices and Research (including Long COV… [isz2IQs_EPg]Evidence Quote
“the FDA have categorized our devices as lowrisk General Wellness devices in accordance to the fda's draft on General wellness policy on lowrisk devices dated January 20 2015 all Vite devices have been independently TUV certified as safe for Consumer use”
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Photobiomodulation Devices and Research (including Long COVID)— MedCram - Medical Lectures Explained CLEARLYCreated: 8/10/2026, 10:04:37 PM
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