Medical Device Manufacturer · US , Murray , UT

U&I Corp., America - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2003
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
1-3 of 3
Cleared Jun 27, 2003
U&I, OPTIMA, SPINAL SYSTEM
K031585 · MNH
Orthopedic · 37d
Cleared Jun 24, 2003
U & I AMERICA SPINAL HOOK SYSTEM
K031595 · KWP
Orthopedic · 34d
Cleared Mar 12, 2003
OPTIMA, SPINAL SYSTEM
K024096 · MNI
Orthopedic · 90d
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All3 Orthopedic 3