The best LED eye mask

Last reviewed October 2026.

Short answer: of the four LED eye devices we checked, 2 have an FDA 510(k) record that names the product: the CurrentBody LED Eye Perfector (K221444, held by Light Tree Ventures Europe B.V.) and the Solawave Eye Recovery Pro (K261602 and K233556, held by manufacturers, not by the brand). We found no K-number for the Dr. Dennis Gross DRx SpectraLite EyeCare Max Pro or the iRestore Red Light Therapy for Eyes. FDA records read on 16 October 2026. No eye device has an independent light measurement, so this list ranks on the FDA record only. A 510(k) clearance is a safety and equivalence review, not a results guarantee. It is not FDA approval.

The list, by FDA status

How this list is ranked

First by FDA status. A device whose name FDA's registration & listing index ties to a 510(k) clearance ranks above one with no clearance we could find. The CurrentBody LED Eye Perfector ranks first because its Amazon listing also gives a model number that the 510(k) names. The Solawave Eye Recovery Pro listing gives none. Then, within a tier, by irradiance measured in a cited spectrometer test, as on the face-mask list. No such test exists for any of these four eye devices. The makers' own LED counts and output figures are not on the same ruler, so they never rank a device here.

Device by device

• CurrentBody LED Eye Perfector: Cleared — FDA's record ties this product to a K-number held by a manufacturer or licensor. FDA's registration & listing index names the “CurrentBody Skin LED Eye Perfector” and the “CurrentBody Skin LED Eye Mask” under K221444, in the listing of The Beauty Tech Group Ltd (CurrentBody's parent). The site first confirmed this listing name on 8 October 2026 and read it again on 16 October 2026. The Amazon listing gives the item model number CBD-EY-36A. The 510(k) device name covers models EY-36A and EY-36B. Maker's claim: The Amazon listing text we read does not use the words “FDA cleared”. This page answers from the FDA record. Specification: 80 LEDs, 4 wavelengths, 3-minute treatment (Amazon listing, read 16 October 2026; the maker's own figures, not a test).
• Solawave Eye Recovery Pro: Cleared — FDA's record ties this product to a K-number held by a manufacturer or licensor. Two FDA records name this product. Shenzhen Goodwind's registration lists “Solawave eye recovery pro (Model:PH-e03)”, and K261602 (cleared 10 August 2026) is Goodwind's “Eye Recovery Pro (PH-e03)”. Shenzhen Kaiyan's listing under K233556 (cleared 4 January 2024) also names a “Solawave Eye Recovery Pro”. Both clearances are held by the manufacturer, not by Solawave. The Amazon listing (sold by Solawave's own store) gives no model number. Its LED count and wavelengths (80 LEDs; 605, 630, 660 and 830 nm) are the same as on Solawave's own Eye Recovery Pro page. We cannot tell from the listing which of the two FDA records the unit in the box is filed under. Maker's claim: “an FDA-cleared, award-winning hands-free LED eye mask” (solawave.co, Radiant Renewal Eye Recovery Pro product page, read 16 October 2026). Specification: 80 LEDs; 605 nm amber, 630 nm red, 660 nm deep red, 830 nm near-infrared; 3-minute treatment (Amazon listing and Solawave's page, read 16 October 2026; the maker's own figures, not a test).
• Dr. Dennis Gross DRx SpectraLite EyeCare Max Pro: Marketed as FDA cleared; no matching K-number found under the names we checked. No FDA registration & listing name contains “Dennis Gross”, “DRx”, “SpectraLite” or “EyeCare Max” for a light-therapy device. The only SpectraLite in the 510(k) database is K171386, “dpl SpectraLite”, a 2017 clearance held by LED Technologies, Inc., and none of LED Technologies' 15 clearances is an eye device. Maker's claim: “Dermatologist-developed and FDA-cleared” (Amazon listing B0BWPJDQB1, first bullet, read 16 October 2026). Specification: 96 LEDs, 4 wavelengths of red light, 3-minute treatment (Amazon listing, read 16 October 2026; the maker's own figures, not a test).
• iRestore Red Light Therapy for Eyes: No K-number found under the names we checked, and the listing does not claim one. iRestore's FDA records are its hair-growth clearances (product code OAP, held by Freedom Laser Therapy) and listings for its LED belts. No 510(k) or listing name for an iRestore eye device was found. Maker's claim: “manufactured in a GMP certified facility that is also FDA listed” (Amazon listing B0D953MF72, product description, read 16 October 2026). The listing does not say “FDA cleared”. An FDA-listed facility is a registration, not a device clearance. Specification: 180 LEDs, red and infrared light (Amazon listing, read 16 October 2026; the maker's own figures, not a test).

What a clearance does and does not tell you

The product code for these devices is OHS, “Light Based Over The Counter Wrinkle Reduction”. A 510(k) clearance is a safety and equivalence review, not a results guarantee. It is not FDA approval. This site does not say what any device does for the skin around the eyes, and it gives no medical or eye-safety advice. Statements about eye safety are the makers' own claims; read the maker's instructions. The eye-safety record for LED masks and “cleared”, “registered” and “approved” explain the terms.

Sources and dates

• FDA 510(k) record K221444 (read 16 October 2026)
• FDA 510(k) record K233556 (read 16 October 2026)
• FDA 510(k) record K261602 (read 16 October 2026)
• FDA 510(k) database and registration & listing index, searched 16 October 2026: K221444, K261602 and K233556 by number; applicant and device-name searches for Dennis Gross, DRx, EyeCare, SpectraLite, Solawave, iRestore and Freedom Laser Therapy; product code OHS with 'eye' in the device name (3 records: K261602, K221444, K233556); listing names containing 'eye perfector', 'eyecare', 'eyeware', 'solawave', 'irestore', 'dennis', 'drx' and 'spectralite'.
• Amazon US buy boxes, read 16 October 2026 for a delivery address in East Hanover, NJ 07936.

Face masks: the best LED face mask, by measured irradiance · the Dr. Dennis Gross SpectraLite FaceWare Pro record · every mask, claim by claim.

LED Mask Score indexes manufacturers' FDA marketing claims against the FDA's own public record — the 510(k) database and the registration & listing index — with links, so you can read the paper yourself. We test nothing and give no medical or skincare advice. A 510(k) clearance is a safety-and-equivalence review, not a performance ranking, an endorsement, or an "FDA approval." If a brand publishes a K-number or listing that changes a row, the page changes — the record wins.

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