Manufacturer registered with FDA
Huaxian Yuwei Dental Materials Factory
Shangguan Town, Huaxian, Anyang City, 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
- 21 registrations outside the US
- Establishments
- 1China
Registered in 2 markets
Where regulators' registries name Huaxian Yuwei Dental Materials Factory 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 | Huaxian Yuwei Dental Materials Factory | 1 device types | — | Below |
| Brazil | ANVISA | Manufacturer | HUAXIAN YUWEI DENTAL MATERIALS FACTORY | 1 | 2024–2024 | 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 Huaxian Yuwei Dental Materials Factory currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Teeth Plastic DentureELM · Class 2 | Denture resins & teeth | Maker | Yuwei Brand Synthetic Polymer Teeth (Ecostar,Suplar.Neputas,Physioca,Typlus)Yuwei Brand Synthetic Polymer Teeth (Mercury, Venus, Mars, Jupiter, Saturn, Uranus, Neptune ) | 2015 |
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 |
|---|---|---|
| Huaxian Yuwei Dental Materials FactoryFDA reg. 3009541709 | Anyang City Henan, China | Contract manufacturer, Contract sterilizer, Foreign exporter, Manufacturer, Repacker / relabeler, Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10039901). 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.