Renovo Life, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renovo Life, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Renovo Life, LLC has 2 FDA 510(k) cleared medical devices. Based in Belmont, US.
Historical record: 2 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Renovo Life, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Renovo Life, LLC
2 devices