Not currently registered with FDA under this name

Amann Girrbach America, Inc.

Deer Field, IL, United States. Named as applicant on 1 dental 510(k) clearance between 2007 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12007–2007
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Amann Girrbach America, Inc. as the applicant.

Decided	510(k)	Device	Device type
2 Feb 2007	K063511	CERAMILL ZI	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.