Medo U.S.A., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medo U.S.A., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Medo U.S.A., Inc. has 2 FDA 510(k) cleared medical devices. Based in Wood Dale, US.
Historical record: 2 cleared submissions from 1984 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medo U.S.A., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medo U.S.A., Inc.
2 devices