Lumenr, LLC is one of 17582 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lumenr, LLC - FDA 510(k) Cleared Devices
Recent clearances: LumenR Tissue Retractor System
1
Total
1
Cleared
0
Denied
Lumenr, LLC has 1 FDA 510(k) cleared medical devices. Based in Matawan, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Lumenr, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Joseph Azary as regulatory consultant.
FDA 510(k) Regulatory Record - Lumenr, LLC
1 devices