Not currently registered with FDA under this name

Drfp , Ltd.

Amsterdam, United Kingdom. Named as applicant on 2 dental 510(k) clearances between 2010 and 2012. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 22010–2012
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Drfp , Ltd. as the applicant.

Decided	510(k)	Device	Device type
20 Jun 2012	K120048	DRFP PROPOINTS, PROPOINTS 4%, PROPOINTS 6%, PROPOINTS PT, PROPOINTS S	KIF Root Canal Filling Resin
22 Oct 2010	K100248	DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S	KIF Root Canal Filling Resin

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.