Manufacturer registered with FDA
Shenzhen Yuxinyuan Electronic Technology Co., Ltd.
Shenzhen, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 22 registrations outside the US
- Establishments
- 1China
Registered in 2 markets
Where regulators' registries name Shenzhen Yuxinyuan Electronic Technology Co., Ltd. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Shenzhen Yuxinyuan Electronic Technology Co., Ltd. | 1 device types | — | Below |
| Canada | Health Canada | Registration holder | SHENZHEN YUXINYUAN ELECTRONIC TECHNOLOGY CO., LTD. | 2 | 2025–2026 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Shenzhen Yuxinyuan Electronic Technology Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Oral Irrigation UnitEFS · Class 1 | Oral irrigators | Maker | Power Oral Irrigators:YXY-801,YXY-802,YXY-803,YXY-8031,Y820,YXY-821,Y201,Y201B,Y202,Y205,Y206,Y207,Y208,Y209,Y215YXY-880,Y881,Y825,Y826,P20,Y601,Y211,Y212,Y213,Y702, Y255 | 2019 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| Shenzhen Yuxinyuan Electronic Technology Co., Ltd.FDA reg. 3013826894 | Shenzhen Guangdong, China | Contract manufacturer, Foreign exporter, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10061241). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.