Not currently registered with FDA under this name
Jaintek Co.,Ltd
Ansan-Si, South Korea. Named as applicant on 1 dental 510(k) clearance between 2022 and 2022. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 12022–2022
- Markets registered in
- 411 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2007–2026
Registered in 4 markets
Where regulators' registries name Jaintek Co.,Ltd as the manufacturer or the registration holder of a device.
RegisteredHome: South KoreaOne marker per market
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Jaintek Co.,Ltd | 1 clearances | 2022–2022 | Below |
| European Union | EUDAMED | Manufacturer | Jaintek Co., Ltd. | 6 | — | Pure Global AI |
| Australia | TGA | Manufacturer | Jaintek Co Ltd | 3 | 2022–2025 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | Jaintek Co., Ltd | 2 | 2022–2024 | 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
Sources
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 of the most recent filing, which can be a US agent.