Sonowand AS
Country not established
- Devices
- 2
What Sonowand AS makes
Sonowand AS manufactures accessories for ultrasound-guided procedures, including general-purpose localizers and adapters designed to enhance the functionality of their Sonowand system. The Sonowand Invite is a key product, likely intended for procedural guidance in medical imaging.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) premarket notifications. The company is based in the United States and has its products listed in the FDA’s 510(k) registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Sonowand Invite Ref K083597
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonowand AS have in the registry?
The registry currently lists 2 devices for Sonowand AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonowand AS's devices?
Among its 2 most recently registered devices, Sonowand AS has devices listed in FDA 510(k) (2 devices).
What risk classes do Sonowand AS's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sonowand AS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonowand AS in the registry?
The most recently registered devices listed for Sonowand AS include GENERAL PRUPOSE LOCALIZERS AND ADAPTERS-NEW ACCESSORIES FOR SONOWAND SYSTEM and SONOWAND INVITE.