The Beauty Tech Group Ltd

FDA Device Registration & Listing · Macclesfield Cheshire East, GB · Registration 3014737458

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014737458
FEI Number
3014737458
Entity Name
The Beauty Tech Group Ltd
City/State/Country
Macclesfield Cheshire East, GB
Establishment Address
Glasshouse, Suite 3F1, Congleton Road, Nether Alderley, Macclesfield Cheshire East SK10 4ZE, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Currentbody Ltd. (Owner Number: 10060586)
Owner / Operator Contact Address
Glasshouse, Block 1s1, Congleton Road, Nether Alderley, Macclesfield, GB-CHE SK10 4ZE, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230090
PMA Number
N/A

All Registered Proprietary Names

Omnilux contour Facelite rio UNveiLED Skinlite Currentbody Skin Facelite Light salon Boost My LED ZIIP HALO CurrentBody Skin Anti-Acne LED Mask - US (Blue/Red) CurrentBody Wellness Recovery Boots TRIA 4X HRL4x Currentbody Skin RF CurrentBody Skin Radio Frequency Device CurrentBody Skin LED Eye Perfector CurrentBody Skin LED Eye Mask CurrentBody Hair Helmet (Large) CurrentBody Skin LED Hair Regrowth CurrentBody Hair Helmet (Medium) Currentbody LED Lip Perfector CURRENTBODY Dermalux Flex MD SRL Powered Laser Surgical Instrument With MicrobeamFractional Output TRIA FRX Currentbody CURRENTBODY SKIN LED Light Therapy Mask series 2 CurrentBody Skin LED Light Therapy Mask: Sonia Edition (2025) CURRENTBODY Skin 4-IN-1 LED FACE MASK CurrentBody Skin Laser Hair Removal Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2020-04-27
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes Neurology Class 2 882.5890 2024-02-23
OLP Over-The-Counter Powered Light Based Laser For Acne General, Plastic Surgery Class 2 878.4810 2024-02-01
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2024-02-01
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2025-03-17
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2020-08-25
PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction General, Plastic Surgery Class 2 878.4420 2024-05-24
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2023-01-16
OAP Laser, Comb, Hair Physical Medicine Class 2 890.5500 2023-05-25
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2023-05-09
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2023-05-09
OLP Over-The-Counter Powered Light Based Laser For Acne General, Plastic Surgery Class 2 878.4810 2021-12-06
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2021-12-06
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2021-12-06
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output General, Plastic Surgery Class 2 878.4810 2020-08-27
OHS Light Based Over The Counter Wrinkle Reduction General, Plastic Surgery Class 2 878.4810 2023-01-16
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2023-10-13

Official Correspondent

No official correspondent registered.

US Agent Details

Wen Wang Business: Willow Glen Consultancy LLC Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

Currentbody Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3029083714 The Beauty Tech Group LLC Pleasant Hill, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K242140 Jiale Health Technology Shenzhen Co., Ltd. Air Compression Leg Massager (K-705) 2025-03-17
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26
K202758 Shangdong Huamei Technology Co., Ltd. Nd: YAG Laser Therapy Systems HM-YL900 2020-11-16
K904068 Luxar Corp. LUXAR MODEL LX-20 CO2 LASER 1991-04-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007 Lumenis Inc. 2
Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014737458. Last updated year: 2026. Please use registration number 3014737458 when referencing this establishment in official correspondence.
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