Fuselier Enterprises, LLC is one of 4733 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fuselier Enterprises, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Fuselier Enterprises, LLC has 1 FDA 510(k) cleared medical devices. Based in Maitland, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Fuselier Enterprises, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fuselier Enterprises, LLC
1 devices