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LightStim LightStim for Wrinkles (handheld)

Product image: LightStim product page.
LightStim for Wrinkles is a handheld LED paddle, not a mask: you hold it over one area at a time.
It has 72 LEDs across amber, light red, dark red and infrared light (605, 630, 660 and 855 nm). The brand says a charge gives 2 hours of use, or about 40 treatment areas at 3 minutes each. It's FDA-cleared (latest 510(k) K261482).
It's the lowest-priced device with a matched 510(k) in our LED list, and its size suits spot use or travel. The downside is time: covering your whole face area by area takes much longer than wearing a mask.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| LightStim (brand site) | $269 | Nov 1, 2026 brand store data |
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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. 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
| Format | Handheld paddle, not a mask |
|---|---|
| Wavelengths | 605 nm, 630 nm, 660 nm, 855 nm source |
| 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) K261482 510(k) 'LightStim for Wrinkles (1984); LightStim for Acne (2038)', decided 2026-07-31. Earlier OTC clearance K101190 (2010). 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
- nm
- Nanometres, the unit for a light's wavelength (its colour). Red light is roughly 620–700 nm; near-infrared is above 700 nm.
- 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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