Levo USA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Levo USA - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Levo USA has 4 FDA 510(k) cleared medical devices. Based in Dottikon, CH.
Historical record: 4 cleared submissions from 1996 to 1997. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Levo USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Levo USA
4 devices