Renovo Life, LLC is one of 18489 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
Recent clearances: Renovo Life Small Bone IM Nail System, Renovo Life Hard Carbon Coated Drill Bit
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.
510(k) submissions have been managed by Orgenix, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Renovo Life, LLC
2 devices