Medical Device Manufacturer · US , Prescott , WI

Cerabio, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

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

1-2 of 2