Not currently registered with FDA under this name

Caulk Co., Div. Dentsply

Walker, MI, United States. Named as applicant on 2 dental 510(k) clearances between 1979 and 1981. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 21979–1981
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1976–2026

510(k) clearances

Clearances on which FDA names Caulk Co., Div. Dentsply as the applicant.

Decided	510(k)	Device	Device type
8 Sep 1981	K812277	PRISMA-FIL COMPULES	EID Restorative and Impression Material Syringe
26 Jan 1979	K782080	VENEER SYSTEM, MOSTIQUE LAMINATE	KLE Resin Tooth Bonding Agent

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.