Nexus CMF, LLC is one of 25895 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nexus CMF, LLC - FDA 510(k) Cleared Devices
Recent clearances: TruVision Single-Use 1.9mm Arthroscopy System
1
Total
1
Cleared
0
Denied
Nexus CMF, LLC has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Nexus CMF, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mededge Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Nexus CMF, LLC
1 devices