Reoss GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Reoss GmbH - FDA 510(k) Cleared Devices
Recent clearances: Yxoss CBR®
1
Total
1
Cleared
0
Denied
Reoss GmbH has 1 FDA 510(k) cleared medical devices. Based in Filderstadt, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Reoss GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Confinis as regulatory consultant.
FDA 510(k) Regulatory Record - Reoss GmbH
1 devices