Medical Device Manufacturer · US , Ponte Vedra , FL

Mmi North America, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2024

1

Total

0

Cleared

1

Denied

FDA 510(k) Regulatory Record - Mmi North America, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Not Cleared Apr 05, 2024

Symani Surgical System

DEN230032 · SAQ

General & Plastic Surgery · 346d