Levo USA
SwitzerlandFDA applicant, unverified
- Devices
- 4
What Levo USA makes
Levo USA manufactures manual lumbar and cervical traction devices, including portable models like the LEVO MOBIL LCM and stationary units such as the LEVO ACTIVE-EASY LAE and LEVO COMPACT-EASY LCE. These devices are designed for clinical and home use to apply controlled traction for spinal decompression.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. Levo USA operates from the United States.
Catalogue
Levo Mobil Lcm Ref K963817
Regimes: 510(k) Registry: 510(k)Levo Active-Easy Lae Ref K971873
Regimes: 510(k) Registry: 510(k)Levo Compact-Easy Lce Ref K973951
Regimes: 510(k) Registry: 510(k)Levo Compact Lc Ref K963816
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Levo USA have in the registry?
The registry currently lists 4 devices for Levo USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Levo USA's devices?
Among its 4 most recently registered devices, Levo USA has devices listed in FDA 510(k) (4 devices).
What risk classes do Levo USA's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Levo USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Levo USA in the registry?
The most recently registered devices listed for Levo USA include LEVO MOBIL LCM, LEVO ACTIVE-EASY LAE, LEVO COMPACT-EASY LCE and LEVO COMPACT LC.