Nelis is one of 18943 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nelis - FDA 510(k) Cleared Devices
Recent clearances: Endo Keeper, GLOVE PORT
2
Total
2
Cleared
0
Denied
Nelis has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Nelis Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Plusglobal as regulatory consultant.
FDA 510(k) Regulatory Record - Nelis
2 devices