Ultrazonix Dnt AB
Country not established
- Devices
- 1
What Ultrazonix Dnt AB makes
Ultrazonix Dnt AB manufactures the Spine Minimal-Invasive Disc System, a device designed for spinal disc procedures requiring less invasive techniques.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device. The system is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Ultrazonix Spine Minimal-Invasive Disc System Ref K060346
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultrazonix Dnt AB have in the registry?
The registry currently lists 1 device for Ultrazonix Dnt AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultrazonix Dnt AB's devices?
Among its 1 most recently registered device, Ultrazonix Dnt AB has devices listed in FDA 510(k) (1 device).
What risk classes do Ultrazonix Dnt AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultrazonix Dnt AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultrazonix Dnt AB in the registry?
The most recently registered devices listed for Ultrazonix Dnt AB include ULTRAZONIX SPINE MINIMAL-INVASIVE DISC SYSTEM.