Avalon Biomed, Inc. is one of 4765 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avalon Biomed, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Avalon Biomed, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bradenton, US.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Avalon Biomed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avalon Biomed, Inc.
3 devices