Data / Medical devices / United Kingdom / The Beauty Tech Group Ltd
The Beauty Tech Group Ltd: FDA-registered device maker in Macclesfield Cheshire East, United Kingdom, 17 510(k) clearances
The Beauty Tech Group Ltd is registered with the FDA (registration 3014737458) in Macclesfield Cheshire East, United Kingdom. It lists 11 device types. The FDA files 17 510(k) clearances under its listings, the newest dated June 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014737458
- Address
- Glasshouse, Suite 3F1, Congleton Road Nether Alderley, Macclesfield Cheshire East, United Kingdom, SK10 4ZE
- Owner or operator
- Currentbody Ltd. (10060586)
- Roles
- Exporter to the US, Specification developer
- First device listed
- April 27, 2020
- Registered through
- 2026
- Brand names listed
- CURRENTBODY, CURRENTBODY SKIN LED Light Therapy Mask series 2, CURRENTBODY SKIN LED MULTI-LIGHT THERAPY MASK, CURRENTBODY Skin 4-IN-1 LED FACE MASK, CurrentBody Hair Helmet (Large), CurrentBody Hair Helmet (Medium), CurrentBody LED Light Therapy Mask: Series 3, CurrentBody LED Teeth Whitening Device and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 3, 2026 | K260715 | CurrentBody Skin LED Multi Light Therapy Mask (MK-110D) | OHS | Substantially Equivalent | The Beauty Tech Group, Ltd. | accessdata.fda.gov |
| June 17, 2025 | K251017 | CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) | OAP | Substantially Equivalent | Shenzhen Kaiyan Medical Equipment Co., Ltd. | accessdata.fda.gov |
| February 19, 2025 | K243206 | Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) | IRP | Substantially Equivalent | Sichuan Qianli-Beoka Medical Technology, Inc. | accessdata.fda.gov |
| February 14, 2025 | K242593 | CurrentBody LED 4 in 1 Zone Facial Mapping Mask (MK-90C, MK-90M, MK66RB-F, MK-90N) | OHS | Substantially Equivalent | Shenzhen Kaiyan Medical Equipment Co., Ltd. | accessdata.fda.gov |
| March 6, 2024 | K232424 | CurrentBody Skin RF | PAY | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| April 19, 2023 | K230090 | Diode Laser Hair Removal | OHT | Substantially Equivalent | Wuhan Lotuxs Technology Co., Ltd. | accessdata.fda.gov |
| April 5, 2023 | K230336 | CurrentBody Skin Led Hair Regrowth(Model: MZ-07) | OAP | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| March 9, 2023 | K223642 | LED Lip Perfector, model: ZC-05 | ILY | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| December 20, 2022 | K221775 | LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| December 8, 2022 | K221444 | LED Eye Perfector, model: EY-36A, EY-36B | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| November 22, 2022 | K221946 | LED Light Therapy Mask (model: MK66R-B) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| November 18, 2021 | K212275 | Dermalux Flex MD | OHS | Substantially Equivalent | Aesthetic Technology, Ltd. | accessdata.fda.gov |
| September 23, 2021 | K212342 | ZIIP+ Device | NFO | Substantially Equivalent | Ziip, Inc. | accessdata.fda.gov |
| July 21, 2021 | K203271 | Aduro light therapy Handheld | OLP | Substantially Equivalent | Shenzhen Kaiyan Medical CO , Ltd. | accessdata.fda.gov |
| September 12, 2019 | K191629 | faceLITE | OHS | Substantially Equivalent | Ismart Marketing Svcs, Ltd. | accessdata.fda.gov |
| October 25, 2013 | K130459 | TRIA FAN SYSTEM | ONG | Substantially Equivalent | Tria Beauty, Inc. | accessdata.fda.gov |
| December 23, 2009 | K090820 | TRIA HAIR REMOVAL LASER SYSTEM | GEX | Substantially Equivalent | Spectragenics, Inc. | accessdata.fda.gov |
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Updated June 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.