Not currently registered with FDA under this name

Zxtgy (Beijing) Technology Co., Ltd.

Beijing, China. Named as applicant on 1 dental 510(k) clearance between 2017 and 2017. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12017–2017
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Zxtgy (Beijing) Technology Co., Ltd. as the applicant.

Decided	510(k)	Device	Device type
28 Nov 2017	K161652	DIAZIR	EIH Porcelain Powder

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.