Levo Medical Corporation
Country not established FDA establishment FEI 3020982310
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Levo Gen 2 Tinnitus Therapy System Ref K260413
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020982310
- Address
- 455 Boleskine Road, Victoria British Columbia
FDA establishments
- Levo Medical Corporation US
Frequently asked questions
How many devices does Levo Medical Corporation have in the registry?
The registry currently lists 1 device for Levo Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Levo Medical Corporation's devices?
Among its 1 most recently registered device, Levo Medical Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Levo Medical Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Levo Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Levo Medical Corporation in the registry?
The most recently registered devices listed for Levo Medical Corporation include Levo Gen 2 Tinnitus Therapy System.
Which FDA establishments are linked to Levo Medical Corporation?
1 FDA establishment is linked to Levo Medical Corporation in the registry; they are listed on the company page.