Dunamis Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dunamis Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Dunamis Screw and Suture Locking System
1
Total
1
Cleared
0
Denied
Dunamis Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Greenville, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dunamis Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dunamis Medical, LLC
1 devices