US Bionics, Inc. (Dba Suitx)
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- Devices
- 1
What US Bionics, Inc. (Dba Suitx) makes
Us Bionics, Inc. (Dba Suitx) manufactures the Phoenix, an exoskeleton device designed to assist mobility for individuals with lower-limb disabilities or mobility impairments.
The Phoenix is classified as a Class II medical device in the US and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
Phoenix Ref K183152
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Us Bionics, Inc. (Dba Suitx) have in the registry?
The registry currently lists 1 device for Us Bionics, Inc. (Dba Suitx). Devices recorded under merged duplicate company entries are counted once.
Which registries list Us Bionics, Inc. (Dba Suitx)'s devices?
Among its 1 most recently registered device, Us Bionics, Inc. (Dba Suitx) has devices listed in FDA 510(k) (1 device).
What risk classes do Us Bionics, Inc. (Dba Suitx)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Us Bionics, Inc. (Dba Suitx)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Us Bionics, Inc. (Dba Suitx) in the registry?
The most recently registered devices listed for Us Bionics, Inc. (Dba Suitx) include Phoenix.