Monarch Medical Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monarch Medical Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: EndoTool SubQ 2.1, EndoTool IV System, EndoTool IV 1.10
3
Total
3
Cleared
0
Denied
Monarch Medical Technologies, LLC has 3 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Last cleared in 2021. Active since 2020. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Monarch Medical Technologies, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Medical Device Academy.
FDA 510(k) Regulatory Record - Monarch Medical Technologies, LLC
3 devices