Data / Medical devices / China / Zhongshan Sunclean Co.,ltd
Zhongshan Sunclean Co.,ltd: FDA-registered device maker in Zhongshan Guangdong, China, 1 510(k) clearance
Zhongshan Sunclean Co.,ltd is registered with the FDA (registration 3018520804) in Zhongshan Guangdong, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 29, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018520804
- Address
- F/5, F/6 #1, F/7, F/8 #2 & F/9,Building G, NO.3 of Huanzhen North 13 RD, Henglan Town, Zhongshan, Guangdong, Zhongshan Guangdong, China, 528478
- Owner or operator
- Zhongshan Sunclean Co.,Ltd (10083364)
- Roles
- Manufacturer
- First device listed
- November 15, 2021
- Registered through
- 2026
- Brand names listed
- 59S Instant Disinfection Fixture,L1000,L2000, 59S SUNCLEAN LIGHTING 3-IN-1 LED Downlight,SZS16-D10-6,SZS18-D10-8,SZS12-D10-4U,SZS12-D10-6U,SZS9-D20-25, 59S SUNCLEAN LIGHTING 3-IN-1 LED Downlight,SZS16-D30-16,SZS25-D30-25,SZS25-X20, SZS25-X30,SZS25-X33, 59S SUNCLEAN LIGHTING 3-IN-1 LED Downlight,SZS6-D20-4,SZS6-D20-4S,SZS6-D20-5,SZS8-D20-6,SZS9-D20-8, 59S SUNCLEAN LIGHTING 3-IN-1 LED Downlight,SZS9-D40-25,SZS9-D20-3,SZS9-D40-3,SZS9-D20-25S,SZS6-D20-25, 59S SUNCLEAN LIGHTING 3-IN-1 LED Panel Light,SZS12-P10-3030,SZS16-P10-3030B,SZS12-P10-3060,SZS16-P10-3060B, 59S SUNCLEAN LIGHTING 3-IN-1 LED Panel Light,SZS18-P10-60120, 59S SUNCLEAN LIGHTING 3-IN-1 LED Panel Light,SZS18-P10-6060,SZS24-P10-6060B,SZS18-P 10-30120,SZS36-P10-30130 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Disinfector, Medical Devices | MEC | 2 | Manufacturer | accessdata.fda.gov |
| Respiratory Accessory Microbial Reduction Device. | QXQ | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile | NOB | 1 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| April 29, 2026 | K252471 | Paptizer 360 | QXQ | Substantially Equivalent | LiViliti Health Products Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Respiratory Accessory Microbial Reduction Device.
- All makers of Disinfector, Medical Devices
- All makers of Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile
Updated April 29, 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.