Manufacturer registered with FDA
Shanghai Joy Crown Industry Co., Ltd
Pu Dong New Area, China. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 312 registrations outside the US
- Establishments
- 1China
Registered in 3 markets
Where regulators' registries name Shanghai Joy Crown Industry 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 | Shanghai Joy Crown Industry Co., Ltd | 4 device types | — | Below |
| European Union | EUDAMED | Manufacturer | SHANGHAI JOY CROWN INDUSTRY CO., LTD. | 10 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | SHANGHAI JOY CROWN INDUSTRY CO., LTD | 2 | 2017–2017 | 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 Shanghai Joy Crown Industry 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 |
|---|---|---|---|---|
| Dental NeedleDZM · Class 1 | Dental needles & syringes | Maker | JOY155 | 2022 |
| Air and/or Water Syringe UnitECB · Class 1 | Dental hand instruments | Maker | JOY133 | 2022 |
| Roll CottonEFN · Class 1 | — | Maker | JOY135 | 2022 |
| Paper Saliva AbsorberKHR · Class 1 | — | Maker | JOY137 | 2022 |
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 |
|---|---|---|
| Shanghai Joy Crown Industry Co., LtdFDA reg. 3010198795 | Pu Dong New Area Shanghai, China | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10085233). 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.