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Omnilux Clear (red + blue)

Omnilux Clear (red + blue) product photo

Product image: Omnilux product page.

Omnilux Clear is a face mask that combines blue and red LED light and is designed for blemish-prone skin.

Blue light is the part aimed at breakouts; red light is included alongside it. We matched it by name to a 510(k) record (K210948, 2021). A 510(k) is the FDA clearance route for devices similar to ones already on the market.

The brand positions it for breakouts rather than fine lines. If anti-ageing is your main goal, the brand's Contour range uses red and near-infrared instead. We don't have a published power figure or LED count for the Clear model yet.

Lowest price we saw (price checked Nov 1, 2026)$395
FDA-cleared

Prices

StorePricePrice checked / source
Omnilux (brand site)$395 Nov 1, 2026
brand store data		 View
Sephora$395 Nov 1, 2026
retailer catalog		 View

Store links go straight to the store's product page, with no affiliate tracking. Confirm the price there before you buy. See our disclosure.

Price history

We don't have a sourced price history for this device yet. The prices above are what we saw on the dates shown. A current sale price isn't necessarily the lowest this device has sold for.

Specs & regulatory status

Wavelengthsnot listed
Power claimed (irradiance)not published by the brand
Power measured (available third-party measurement)No third-party measurement found yet.
FDA statusFDA-cleared 510(k) K210948
510(k) 'Omnilux CLEAR', Globalmed Technologies, decided 2021-06-24.
FDA record or source

"FDA-cleared" means we matched this product to a 510(k) record: the FDA cleared it as substantially equivalent to an existing device for its labelled use. FDA clearance is not FDA approval, and a listed specification isn't proof that a device works. How we check FDA status.

Terms on this page

mW/cm²
Milliwatts per square centimetre: how much light power reaches each square centimetre of skin (irradiance).
510(k)
The FDA premarket notification route. A cleared 510(k) means the FDA found the device substantially equivalent to one already on the market. It is not FDA approval.