Riemser Arzneimittel AG

Riemser Arzneimittel AG holds 3 FDA 510(k) medical device clearances, first cleared 2012, most recent 2013.

Top product codes for Riemser Arzneimittel AG

DZE — Dental2 devices
NPM — Dental1 device

Recent clearances by Riemser Arzneimittel AG

K113539 — REVOIS PRO IMPLANT STSYEMCode DZE·2013-05-03
K113042 — REVOIS IMPLANT SYSTEMCode DZE·2013-03-08
K120152 — CERASORB PLUSCode NPM·2012-08-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.