Healing Rayz
This device may be used to provide temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain or muscle spasm.
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.
| 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
| Listed by | Quasar Bio-Tech Inc, United States |
|---|---|
| FDA product code | ILY |
| Device type | Lamp, Infrared, Therapeutic Heating |
| Device class | Class 2 |
| Regulation | 21 CFR 890.5500 |
| Establishment | Specification developer, Manufacturer |
| Record published | 2016-09-19 |
| Record revised | 2020-07-07 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Over the counter | Yes |
| Label carries | lot or batch number, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DPA-027 | In distribution |
Same 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
3 of these are Class II. Class II means a temporary or reversible health consequence. 3 are recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2012-10-25 | Class II | No Marketing Application | Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the device is unapproved. | 7,734 devices total (included in batches identified for the | 2013-05-21 |
| 2012-10-25 | Class II | No Marketing Application | Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the device is unapproved. | 7,734 devices total | 2013-05-21 |
| 2012-10-25 | Class II | No Marketing Application | Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar Power Pack, and Quasar MD because the device is unapproved. | 7,734 devices total | 2013-05-21 |
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.