Manufacturer registered with FDA
Dongguan Yingfeng Metal & Plastic Products Co., Ltd
Dongguan, China. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 21 registrations outside the US
- Establishments
- 1China
Registered in 2 markets
Where regulators' registries name Dongguan Yingfeng Metal & Plastic Products 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 | Dongguan Yingfeng Metal & Plastic Products Co., Ltd | 3 device types | — | Below |
| Australia | TGA | Manufacturer | Dongguan Yingfeng Metal & Plastic Products Co Ltd | 1 | 2020–2020 | 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 Dongguan Yingfeng Metal & Plastic Products 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 |
|---|---|---|---|---|
| Electrode Gel for Pulp TesterEAS · Class 1 | — | Lister | Conductive Gel for external use | 2021 |
| Massaging PickJET · Class 1 | Floss & interdental cleaners | Maker | Dental Polisher | 2024 |
| Ultraviolet Sanitation/Sterilization (for Toothbrushes) Unit Non-SterileNOB · Class 1 | — | Maker | Pioneering earplugs encased in a UV sanitizer | 2024 |
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 |
|---|---|---|
| DONGGUAN YINGFENG METAL & PLASTIC PRODUCTS CO., LTDFDA reg. 3015977541 | Dongguan Guangdong, China | Foreign exporter, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10061441). 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.