Crux Biomedical is one of 20494 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crux Biomedical - FDA 510(k) Cleared Devices
Recent clearances: CRUX VENA CAVA FILTER SYSTEM, CRUX VENA CAVA FILTER SYSTEM
2
Total
2
Cleared
0
Denied
Crux Biomedical has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Crux Biomedical Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Crux Biomedical
2 devices