Medical Device Manufacturer · US , Reno , NV

Inner Act, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Recent clearances: ACNELIFT

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Inner Act, LLC General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jul 27, 2004

General & Plastic Surgery · 91d