Medical Device Manufacturer · US , Greenville , AL

Dunamis Medical, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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
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