Neurolumen, LLC is one of 18972 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurolumen, LLC - FDA 510(k) Cleared Devices
Recent clearances: NEUROLUMEN PN-1000, NEUTROLUMENPN SYSTEM, MODEL 1000
2
Total
2
Cleared
0
Denied
Neurolumen, LLC has 2 FDA 510(k) cleared medical devices. Based in Yukon, US.
Historical record: 2 cleared submissions from 2009 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Neurolumen, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Systec Engineering, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Neurolumen, LLC
2 devices