Manufacturer registered with FDA
Da Chung Medical Co., Ltd.
Dong-Shan, Taiwan. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 657 registrations outside the US
- Establishments
- 1Taiwan
Registered in 6 markets
Where regulators' registries name Da Chung Medical 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 | Da Chung Medical Co., Ltd. | 1 device types | — | Below |
| Saudi Arabia | SFDA | Manufacturer | DA CHUNG MEDICAL CO., LTD. | 39 | — | Pure Global AI |
| Canada | Health Canada | Registration holder | DA CHUNG MEDICAL CO., LTD. | 12 | 2010–2010 | Pure Global AI |
| European Union | EUDAMED | Manufacturer | DA CHUNG MEDICAL CO., LTD. | 4 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | Da Chung Medical Co., Ltd. | 1 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | Da Chung Medical Co.Ltd. | 1 | 2016–2016 | 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 Da Chung Medical 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 FlossJES · Class 1 | Floss & interdental cleaners | Maker | 3M ESPE Floss and Toss | 2017 |
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 |
|---|---|---|
| DA CHUNG MEDICAL CO., LTD.FDA reg. 3007421188 | Dong Shan Township Yilan, Taiwan | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10027896). 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.