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Solawave Radiant Renewal 2-in-1 Skincare Mini

Solawave Radiant Renewal 2-in-1 Skincare Mini product photo

Product image: Solawave product page.

The Solawave 2-in-1 Skincare Mini is a small handheld device that combines red (630 nm) and near-infrared (830 nm) light with gentle warmth.

You use it for 3 minutes per area; lights flash when it's time to move, and it shuts off after 12 minutes. The brand says a charge lasts up to 60 minutes, and a storage bag is included. The FDA record shows a 510(k) clearance (K250532).

It's the lower-priced of the two wands we list and the only one with near-infrared light. It has no current or vibration, and its light output isn't published.

Lowest price we saw (price checked Nov 1, 2026)$119
FDA-cleared

Prices

StorePricePrice checked / source
Solawave (brand site)$119 Nov 1, 2026
brand store data		 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

FormatHandheld mini device
What it doesRed light, Near-infrared, Warmth source
FormatHandheld mini device
Session (brand guidance)12 min (3 min per area), 3–5× a week
BatteryRechargeable; up to 60 min
In the box / notesStorage bag
Wavelengths630 nm, 830 nm source
FDA statusFDA-cleared 510(k) K250532
510(k) 'Solawave 2-in-1 Skincare Mini (Model: 61043)', decided 2025-05-22.
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.
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.