Levo AG is one of 134 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Levo AG - FDA 510(k) Cleared Devices
Recent clearances: LEVO MAX, LEVO C3, LEVO COMFORT II
4
Total
4
Cleared
0
Denied
Levo AG has 4 FDA 510(k) cleared medical devices. Based in 5610 Wohlen, CH.
Historical record: 4 cleared submissions from 2003 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Levo AG Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv America, Inc. and Tuv Sud America, Inc..
FDA 510(k) Regulatory Record - Levo AG
4 devices