Ritter Implants GmbH CO KG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ritter Implants GmbH CO KG - FDA 510(k) Cleared Devices
Recent clearances: Ritter Dental Implant System
3
Total
3
Cleared
0
Denied
Ritter Implants GmbH CO KG has 3 FDA 510(k) cleared medical devices. Based in Monroe, US.
Historical record: 3 cleared submissions from 2014 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ritter Implants GmbH CO KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ritter Implants GmbH CO KG
3 devices