U&I Corp., America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
U&I Corp., America - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
U&I Corp., America has 3 FDA 510(k) cleared medical devices. Based in Murray, US.
Historical record: 3 cleared submissions from 2003 to 2003. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by U&I Corp., America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - U&I Corp., America
3 devices