Monarch Medical Technologies is one of 16115 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monarch Medical Technologies - FDA 510(k) Cleared Devices
Recent clearances: EndoTool IV (3.1), EndoTool SubQ, ENDO TOOL GLUCOSE MANAGEMENT SYSTEM (EGMS)
3
Total
3
Cleared
0
Denied
Monarch Medical Technologies has 3 FDA 510(k) cleared medical devices. Based in Silver Spring, US.
Latest FDA clearance: Dec 2024. Active since 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Monarch Medical Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Certified Compliance Solutions as regulatory consultant.
FDA 510(k) Regulatory Record - Monarch Medical Technologies
3 devices