Not currently registered with FDA under this name

Riemser Arzneimittel AG

Greifswald-Insel Riems, Germany. Named as applicant on 3 dental 510(k) clearances between 2012 and 2013. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 32012–2013
Markets registered in: 22 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Riemser Arzneimittel AG as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: GermanyOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Riemser Arzneimittel AG	3 clearances	2012–2013	Below
Taiwan	TFDA	Manufacturer	RIEMSER ARZNEIMITTEL AG	2	2012–2012	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Riemser Arzneimittel AG as the applicant.

Decided	510(k)	Device	Device type
3 May 2013	K113539	REVOIS PRO IMPLANT STSYEM	DZE Root-Form Endosseous Implant
8 Mar 2013	K113042	REVOIS IMPLANT SYSTEM	DZE Root-Form Endosseous Implant
13 Aug 2012	K120152	CERASORB PLUS	NPM Animal Source Bone Grafting 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.