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Therabody TheraFace Mask Glo
Product image: Therabody product page.
TheraFace Mask Glo is Therabody's lower-priced LED mask, with 504 red, infrared and blue LEDs plus a gentle scalp massage.
The brand lists red (633 nm), infrared (830 nm) and blue (415 nm) light, with a 12-minute routine that includes vibration. The brand says it's designed to improve the look of fine lines, radiance and breakouts.
It costs less than the original TheraFace Mask and has fewer LEDs. We didn't find a 510(k) that names the Glo, and Therabody doesn't publish its power output. It's also sold at Dermstore.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| Therabody (brand site) | $379.99 | Nov 1, 2026 brand store data |
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| Dermstore 15% off your first Dermstore order with code KRISTIN-R59U · Get the code (new customers only; GlowSpec's founder earns store credit. Disclosure) | $379.99 | Nov 1, 2026 retailer page |
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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 |
|---|---|
| LED count | 504 source |
| Power claimed (irradiance) | not published by the brand |
| Power measured (available third-party measurement) | No third-party measurement found yet. |
| FDA status | No clearance found No matching 510(k) found by product name. |
"No clearance found" means we found no matching record in the FDA's database. That doesn't prove no clearance exists. 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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