Not currently registered with FDA under this name

Dentaim Co., Ltd.

Seoul, South Korea. Named as applicant on 1 dental 510(k) clearance between 2009 and 2009. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12009–2009
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Dentaim Co., Ltd. as the applicant.

Decided	510(k)	Device	Device type
26 Jan 2009	K083201	ZMATCH BLOCK	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.