Specialities Remeex International, S.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Specialities Remeex International, S.L. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Specialities Remeex International, S.L. has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 3 cleared submissions from 2004 to 2006. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Specialities Remeex International, S.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Specialities Remeex International, S.L.
3 devices