Nemera is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nemera - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Nemera has 1 FDA 510(k) cleared medical devices. Based in Buffalo Grove, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nemera Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nemera
1 devices