Is the CurrentBody Series 3 FDA cleared?
Last reviewed October 2026.
Yes. FDA's record ties the CurrentBody LED Light Therapy Face Mask: Series 3 to 510(k) K260715, held by The Beauty Tech Group, Ltd., CurrentBody's parent company. FDA's registration & listing index lists The Beauty Tech Group Ltd's products "CurrentBody Skin LED Multi Light Therapy Mask" and "CurrentBody LED Light Therapy Mask: Series 3" under K260715, for product codes OHS and OLP. The 510(k) itself names the device “CurrentBody Skin LED Multi Light Therapy Mask (MK-110D)”. Read in FDA's database on 18 October 2026. A 510(k) clearance is a safety and equivalence review, not a results guarantee. It is not FDA approval.
The Series 2 has its own page. It is not available new on Amazon US at our 18 October 2026 check.
The record on file
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| FDA status | Brand-held K — the holder is CurrentBody's parent company, The Beauty Tech Group |
| 510(k) | K260715 · decided 3 June 2026 · “Substantially Equivalent” · holder The Beauty Tech Group, Ltd. · device name “CurrentBody Skin LED Multi Light Therapy Mask (MK-110D)” |
| Product code | OHS, “Light Based Over The Counter Wrinkle Reduction”; subsequent code OLP |
| Name in FDA's listing | “CurrentBody Skin LED Multi Light Therapy Mask” and “CurrentBody LED Light Therapy Mask: Series 3” (registrant The Beauty Tech Group Ltd, under K260715) |
| Model number | The 510(k) names model MK-110D. The maker's US product page gives the item code CBD-MK-110I (currentbody.us Series 3 product page, read 18 October 2026). Neither source explains the different last letter. |
| Where to buy | Amazon ↗ sold by the brand's own store (The Beauty Tech Group Ltd), in stock at our 18 October 2026 read. |
The cleared use, as FDA's record states it
From the Indications for Use in the K260715 510(k) summary (read 18 October 2026):
- “Mode 1 (including red (633nm), NIR (830nm & 1072nm)) is intended to provide topical heating for the purpose of elevating tissue temperature; for the temporary relief of minor muscle and joint pain, arthritis and muscle spasm; relieving stiffness; promoting the relaxation of muscle tissue; and to temporarily increase local blood circulation.”
- “Mode 2 (including blue (415nm) & red (633nm)) is intended for the treatment of mild to moderate inflammatory acne.”
- “Mode 3 (including yellow (590nm) & NIR (830nm)) is intended for the treatment of full face wrinkles.”
- “The device is intended for use on Fitzpatrick skin types I-IV.”
A 510(k) clearance is a safety and equivalence review, not a results guarantee. It is not FDA approval. This page does not say what the mask does for the skin.
The maker's specs
| The maker's claim | “FDA-cleared LED face mask for advanced anti-aging, clearing, and brightening” (currentbody.us Series 3 product page, read 18 October 2026) |
| Wavelengths | 633 nm red · 830 nm near-infrared · 1072 nm deep near-infrared · 415 nm blue · 532 nm green · 590 nm yellow (currentbody.us Series 3 product page, read 18 October 2026) |
| LED count | 750 LED bulbs (currentbody.us Series 3 product page, read 18 October 2026). The 510(k) summary lists 110 LEDs at each of 415, 532, 590, 633 and 830 nm and 16 LEDs at 1072 nm: 566 in total. (510(k) summary, read 18 October 2026) We do not know why the two counts differ. |
| Session length | 10 minutes (currentbody.us Series 3 product page, read 18 October 2026) |
| Sessions per week | 3 to 5 times a week (currentbody.us Series 3 product page, read 18 October 2026) |
| Modes | 4 preset modes (Advanced Anti-Aging, Advanced Clearing, Complexion Corrector, Balance & Brighten), plus custom modes set in the CurrentBody app (currentbody.us Series 3 product page, read 18 October 2026) |
| Measured irradiance | Not measured. We found no cited third-party irradiance test of the Series 3: the post list of Light Therapy Insiders (the tester the ranking cites) has no Series 3 review at our 2026-10-18 read. The 510(k) summary gives the maker's own output figures; those are declared values, not an independent measurement, so this page does not print them. |
An LED count is not a light measurement. What measured irradiance means.
What changed from the Series 2
| Item | Series 3 | Series 2 |
|---|---|---|
| Wavelengths | 6: red 633 nm, near-infrared 830 nm, deep near-infrared 1072 nm, blue 415 nm, green 532 nm, yellow 590 nm | 3: red 633 nm, near-infrared 830 nm, deep near-infrared 1072 nm |
| LED bulbs (maker's count) | 750 | 236 |
| Preset modes | 4 | 1 |
| MyDose app control of each LED | Yes | No |
| Session (maker's protocol) | 10 minutes, 3 to 5 times a week | 10 minutes, 3 to 5 times a week |
| FDA 510(k) | K260715 (2026), held by The Beauty Tech Group, Ltd. | K250966 (2025), held by Shenzhen Kaiyan Medical Equipment Co., Ltd |
Source: The comparison table on the currentbody.us Series 3 product page, read 2026-10-18, for every row except the FDA row, which is from FDA's database.
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. It is not FDA approval — the three phrases, decoded. CurrentBody's earlier masks ride clearances held by manufacturers — who holds the paper. Adverse-event reports exist for cleared masks — the eye-safety record.
The best LED face mask, by measured irradiance › · every mask, claim by claim
Sources and dates
- FDA 510(k) record K260715 and its 510(k) summary (read 18 October 2026)
- FDA searches: openFDA 510(k) database (device name CurrentBody: 6 records; device name "Series 3": 5 records, none a light-therapy mask; applicant Beauty Tech: 2 records) and FDA's registration & listing index (proprietary name CurrentBody; proprietary name "Series 3"), read 2026-10-18
- currentbody.us Series 3 product page, read 18 October 2026
- Amazon US buy box, read 18 October 2026 for a delivery address in 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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