Fibralign Corporation is one of 20175 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fibralign Corporation - FDA 510(k) Cleared Devices
Recent clearances: BioBridge Collagen Matrix
1
Total
1
Cleared
0
Denied
Fibralign Corporation has 1 FDA 510(k) cleared medical devices. Based in Union City, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Fibralign Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Fibralign Corporation
1 devices