Monarch Bioimplants GmbH is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Monarch Bioimplants GmbH - FDA 510(k) Cleared Devices
Recent clearances: NeuroShield
1
Total
1
Cleared
0
Denied
Monarch Bioimplants GmbH has 1 FDA 510(k) cleared medical devices. Based in Root, CH.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Monarch Bioimplants GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Monarch Bioimplants GmbH
1 devices