Exos, Inc.
Country not established
- Devices
- 1
What Exos, Inc. makes
Exos, Inc. manufactures the Clinical Hand Master System (Model # EXH9000-002), a device designed for upper-limb rehabilitation and functional recovery, likely used in clinical or post-injury therapy settings.
The device is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Clincal Hand Master System Model # EXH9000-002 Ref K922940
510(k) 510(k)
Frequently asked questions
How many devices does Exos, Inc. have in the registry?
The registry currently lists 1 device for Exos, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Exos, Inc.'s devices?
Among its 1 most recently registered device, Exos, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Exos, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Exos, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Exos, Inc. in the registry?
The most recently registered devices listed for Exos, Inc. include CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002.