Nelis is one of 4820 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nelis - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Nelis
2 devices