Ciden Technologies, LLC is one of 5631 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ciden Technologies, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ciden Technologies, LLC has 2 FDA 510(k) cleared medical devices. Based in Bellaire, US.
Historical record: 2 cleared submissions from 2007 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ciden Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ciden Technologies, LLC
2 devices