Ritter Implants GmbH & Co. KG

Ritter Implants GmbH & Co. KG holds 3 FDA 510(k) medical device clearances, first cleared 2014, most recent 2019.

Name variants for Ritter Implants GmbH & Co. KG

as filed with FDA

Ritter Implants GmbH & Co. KG2 devices
Ritter Implants GmbH CO KG1 device

Top product codes for Ritter Implants GmbH & Co. KG

DZE — Dental3 devices

Recent clearances by Ritter Implants GmbH & Co. KG

K180183 — Ritter Dental Implant SystemCode DZE·2019-01-24
K160475 — Ritter Dental Implant SystemCode DZE·2016-12-14
K131557 — RITTER IMPLANT SYSTEMCode DZE·2014-05-09

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