Orthosonix, Inc.
Country not established
- Devices
- 1
What Orthosonix, Inc. makes
Orthosonix, Inc. manufactures the Orthosonix EnergEx, a focused ultrasound device designed for musculoskeletal applications, including targeted tissue treatment to reduce pain and improve function.
The company’s portfolio is regulated under FDA Class II devices, with the EnergEx authorised via 510(k) clearance. The company is headquartered in the United States.
Catalogue
Orthosonix Energex Ref K013094
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthosonix, Inc. have in the registry?
The registry currently lists 1 device for Orthosonix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthosonix, Inc.'s devices?
Among its 1 most recently registered device, Orthosonix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthosonix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthosonix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthosonix, Inc. in the registry?
The most recently registered devices listed for Orthosonix, Inc. include ORTHOSONIX ENERGEX.