Inner Act, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inner Act, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Inner Act, LLC has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Inner Act, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inner Act, LLC
1 devices