Human Extension, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Human Extension, Ltd. makes
Human Extension, Ltd. manufactures the HX Device, a medical product designed for extending limb mobility and function, likely targeting conditions affecting joint range of motion or physical rehabilitation.
The HX Device is classified as a Class II medical device under FDA regulations and is authorised through the 510(k) clearance pathway. The company is based in the United States.
Catalogue
HX Device Ref K173919
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Human Extension, Ltd. have in the registry?
The registry currently lists 1 device for Human Extension, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Human Extension, Ltd.'s devices?
Among its 1 most recently registered device, Human Extension, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Human Extension, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Human Extension, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Human Extension, Ltd. in the registry?
The most recently registered devices listed for Human Extension, Ltd. include HX Device.