Orthodyne, Inc.
Country not established
- Devices
- 1
What Orthodyne, Inc. makes
Orthodyne, Inc. makes medical devices such as the ISKD, which is an intramedullary skeletal kinetic distractor.
The company's portfolio, including devices like the ISKD, is classified as Class II and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthodyne, Inc. have in the registry?
The registry currently lists 1 device for Orthodyne, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthodyne, Inc.'s devices?
Among its 1 most recently registered device, Orthodyne, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthodyne, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthodyne, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthodyne, Inc. in the registry?
The most recently registered devices listed for Orthodyne, Inc. include ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR).