Gradient Technologies, LLC is one of 21528 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gradient Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: QUADRA BLOC TENS PLUS, QUADRA BLOC TENS, MODEL 101
2
Total
2
Cleared
0
Denied
Gradient Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 2 cleared submissions from 2007 to 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Gradient Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gradient Technologies, LLC
2 devices