69 LED Cluster Issue 3

S2110 69 LED Cluster issue 3

Registry build 21.09.26
235manufacturers in China registered for this device type
1catalogue number
9recalls on this code

Who Else Makes It

Concentrated in Guangdong (145), Zhejiang (21), Jiangsu (9). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ILY
Manufacturer City Province Registered as Device types
Zhongshan Chukuang Textile Co., Ltd. Zhongshan Guangdong Contract manufacturer 26
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Shenzhen Kaiyan Medical Equipment Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Dongguan Tutamen Metalwork Co., Ltd. Dongguan Guangdong Contract manufacturer 12
Gymmax Technology Shenzhen Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Xuzhou Kernel Medical Equipment Co Ltd Xuzhou Jiangsu Contract manufacturer 7
Hangzhou Wellbeing Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Wuxi Jiajian Medical Instrument Co., Ltd. Wuxi Jiangsu Contract manufacturer 6
Shenzhen Sungpo HI-Tech Electronic Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Shenzhen Xinlong Precision Plastic Mold Products Co., Ltd. Shenzhen Guangdong Contract manufacturer 4
Shenzhen Allbeauty Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 4

Showing 12 of 235. All 235 manufacturers in China registered for Lamp, Infrared, Therapeutic Heating

Record

Regulatory record for 69 LED Cluster issue 3
Listed by Thor Photomedicine Ltd, United Kingdom
FDA product code ILY
Device type Lamp, Infrared, Therapeutic Heating
Device class Class 2
Regulation 21 CFR 890.5500
Establishment Specification developer, Manufacturer
510(k) K033923
Record published 2025-07-31
Record revised 2026-04-01 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for 69 LED Cluster issue 3
Catalogue number Size Status
3 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Lescolton Shenzhen Lescolton Medical Equipment Co., Ltd. 50
HealthLight Healthlight LLC 40
Therapy Light E.shine Lighting Co., Limited 32
Phoenix Thera-Lase system Phoenix Thera-Lase Systems, LLC 32
AisQueen Shenzhen AIS Queen Medical Technology Co., Ltd. 30
LED RED Light Therapy Panel Shenzhen RedV Medical Equipment Co., Ltd. 27
Chattanooga DJO, LLC 25
Lumix Ultra/Plus Fisioline SRL 22
UTK UTK Technology(Shenzhen)Limited 21
LZ30 Avant Wellness Systems Inc 21
LS Pro Systems Wellness Without Limits LLC 21
Dimed Wuhan Dimed Laser Technology Co., Ltd. 20

Showing 12 of 536. All products under Lamp, Infrared, Therapeutic Heating

Recalls

9 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2025-07-24 Class II Process control The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift. 1 unit
2025-07-24 Class II Process control The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift. 80 units (66 US, 14 OUS)
2025-07-24 Class II Process control The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift. 2 units (1 US, 1 OUS)
2025-07-24 Class II Process control The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift. 55 units (41 US, 14 OUS)
2023-11-20 Class II Component design/selection One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy 61 (41 US; 20 OUS)
2022-09-13 Class II Device Design Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. 6
2022-09-13 Class II Device Design Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. 26
2022-09-13 Class II Device Design Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. 19
2022-09-13 Class II Device Design Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. 26

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer