Medical Device Manufacturer · US , Arlington Heights , IL

Medi USA, LP - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994
4
Total
4
Cleared
0
Denied

Medi USA, LP has 4 FDA 510(k) cleared medical devices. Based in Arlington Heights, US.

Last cleared in 2022. Active since 1994. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Medi USA, LP Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Medi USA, LP
4 devices
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