Medical Device Manufacturer · US , Chicago , IL

Msi - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

1

Total

1

Cleared

0

Denied

Msi has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Msi Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Msi

1 devices

1-1 of 1

Cleared Sep 02, 2022

DURAMESH Mesh Suture

General & Plastic Surgery · 500d