Is the CurrentBody LED Eye Perfector FDA cleared?
Last reviewed October 2026.
Yes. FDA's record ties the CurrentBody LED Eye Perfector to a 510(k) clearance, held by a manufacturer or licensor, not by CurrentBody. 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. Read in FDA's database on 16 October 2026.
The record on file
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| FDA status | OEM-held K — Cleared — FDA's record ties this product to a K-number held by a manufacturer or licensor |
| 510(k) | K221444 · decided 8 December 2022 · holder Light Tree Ventures Europe B.V. · device name “LED Eye Perfector, model: EY-36A, EY-36B” · product code OHS |
| Cleared for | Wrinkles around the eyes (product code OHS) |
| The 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) |
| Where to buy | Amazon ↗ sold by the brand's own store (The Beauty Tech Group Ltd), in stock at our 16 October 2026 read. |
How to read this
“FDA cleared” means a 510(k): the FDA reviewed the device as substantially equivalent to one already on the market and gave it a K-number you can look up. A 510(k) clearance is a safety and equivalence review, not a results guarantee. It is not FDA approval. Many clearances in this category are held by a manufacturer rather than the brand on the box, which is legal and common — who holds the paper. This page does not say what the device does for the skin around the eyes. Statements about eye safety are the maker's own claims; read the maker's instructions and the eye-safety record for LED masks.
All four LED eye devices, ranked by FDA status › · Is the Solawave Eye Recovery Pro FDA cleared? · Is the Dr. Dennis Gross DRx SpectraLite EyeCare Max Pro FDA cleared?
Sources: FDA 510(k) database and registration & listing index, read 16 October 2026; Amazon US buy box, read 16 October 2026 for East Hanover, NJ 07936.
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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