Novasonix Technology S.L.
SpainFDA applicant, unverified
- Devices
- 1
What Novasonix Technology S.L. makes
Novasonix Technology S.L. manufactures the HEBE device, a medical product designed for non-invasive neuromodulation applications, targeting specific neurological or musculoskeletal conditions.
The HEBE device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Hebe (NP0000763) Ref K241733
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Novasonix Technology S.L. have in the registry?
The registry currently lists 1 device for Novasonix Technology S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novasonix Technology S.L.'s devices?
Among its 1 most recently registered device, Novasonix Technology S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Novasonix Technology S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Novasonix Technology S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novasonix Technology S.L. in the registry?
The most recently registered devices listed for Novasonix Technology S.L. include HEBE (NP0000763).