Medical Device Manufacturer · US , Chicago , IL

Msi - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Msi General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared CT Sep 02, 2022

DURAMESH Mesh Suture

General & Plastic Surgery · 500d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 20, 2026