Not currently registered with FDA under this name

Sangi Co., Ltd.

Tokyo, Japan. Named as applicant on 2 dental 510(k) clearances between 2022 and 2026. No establishment is registered with FDA under this exact name today.

2 clearances in five years

Device types listed: 0
Brands and models: 0
510(k) clearances: 22022–2026
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

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

Decided	510(k)	Device	Device type
18 Mar 2026	K260830	APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)	LBH Cavity Varnish
16 Feb 2022	K220419	Apapro Desensitizer	LBH Cavity Varnish

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.