Eele Laboratories, LLC is one of 25747 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eele Laboratories, LLC - FDA 510(k) Cleared Devices
Recent clearances: PLASMACURE BXE
1
Total
1
Cleared
0
Denied
Eele Laboratories, LLC has 1 FDA 510(k) cleared medical devices. Based in Bohemia, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Eele Laboratories, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Eele Laboratories, LLC
1 devices