Not currently registered with FDA under this name

Kuraray Medical Kurashiki Plant

New York, NY, United States. Named as applicant on 2 dental 510(k) clearances between 2004 and 2005. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22004–2005
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Kuraray Medical Kurashiki Plant as the applicant.

Decided	510(k)	Device	Device type
9 Aug 2005	K051796	CLEARFIL TRI-S BOND SINGLE DOSE	KLE Resin Tooth Bonding Agent
6 Dec 2004	K042929	ESTENIA C&B	EBF Resin Tooth Shade Material

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.