Coronet Group North America, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coronet Group North America, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Coronet Group North America, LLC has 1 FDA 510(k) cleared medical devices. Based in Queensbury,, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Coronet Group North America, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coronet Group North America, LLC
1 devices