Not currently registered with FDA under this name

Emergo Europe Consulting

The Hague, Netherlands. Named as applicant on 1 dental 510(k) clearance between 2015 and 2015. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12015–2015
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Emergo Europe Consulting as the applicant.

Decided	510(k)	Device	Device type
21 Sep 2015	K152383	Ceramill Zolid FX	EIH Porcelain Powder

Some of these clearances are listed with FDA today by another company: Amann Girrbach AG (1).

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.