Cerabio, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cerabio, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cerabio, LLC has 2 FDA 510(k) cleared medical devices. Based in Prescott, US.
Historical record: 2 cleared submissions from 2002 to 2002. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cerabio, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cerabio, LLC
2 devices