Medical Device Manufacturer · CH , 5610 Wohlen

Levo AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

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.

Levo AG is one of 86 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

Levo AG — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026