Neomedic International S.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neomedic International S.L. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Neomedic International S.L. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2011 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Neomedic International S.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neomedic International S.L.
2 devices