Orthotone Corp.
Country not established
- Devices
- 1
What Orthotone Corp. makes
Orthotone Corp. manufactures the ORTHOTONE device, which is classified as a Class II medical device.
The company is based in the US and its products are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Orthotone Ref K872111
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthotone Corp. have in the registry?
The registry currently lists 1 device for Orthotone Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthotone Corp.'s devices?
Among its 1 most recently registered device, Orthotone Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthotone Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthotone Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthotone Corp. in the registry?
The most recently registered devices listed for Orthotone Corp. include ORTHOTONE.