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MZ Skin LightMAX Supercharged LED Mask 2.0

Product image: MZ Skin product page.
The MZ Skin LightMAX Supercharged 2.0 is an LED face mask with an anti-ageing mode and an anti-blemish mode.
The anti-ageing mode combines red (633 nm) and near-infrared (830 nm) light. The anti-blemish mode pairs blue (415 nm) with red. The brand describes it as lightweight and breathable for daily use. The FDA record shows a 510(k) clearance (K213184).
At $950 it's the highest-priced mask we list, and MZ Skin doesn't publish its power output or LED count. We couldn't verify specs that explain the price difference.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| Dermstore 15% off your first Dermstore order with code KRISTIN-R59U · Get the code (new customers only; GlowSpec's founder earns store credit. Disclosure) | $950 | Nov 1, 2026 retailer catalog |
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Store links go straight to the store's product page, with no affiliate tracking. Confirm the price there before you buy. The Dermstore code above is our referral code: our founder earns Dermstore store credit when a new customer uses it. 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
| Wavelengths | not listed |
|---|---|
| Power claimed (irradiance) | not published by the brand |
| Power measured (available third-party measurement) | No third-party measurement found yet. |
| FDA status | FDA-cleared 510(k) K213184 510(k) 'MZ Skin LightMAX Supercharged LED Mask 2.0', decided 2021-11-23. 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.
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