Owandar Medical, Ltd.
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
What Owandar Medical, Ltd. makes
Owandar Medical, Ltd. makes the Centrafix External Fixator, which is an orthopedic device used for stabilizing fractures externally.
The Centrafix External Fixator is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Centrafix External Fixator Ref K991732
510(k) 510(k)
Frequently asked questions
How many devices does Owandar Medical, Ltd. have in the registry?
The registry currently lists 1 device for Owandar Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Owandar Medical, Ltd.'s devices?
Among its 1 most recently registered device, Owandar Medical, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Owandar Medical, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Owandar Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Owandar Medical, Ltd. in the registry?
The most recently registered devices listed for Owandar Medical, Ltd. include CENTRAFIX EXTERNAL FIXATOR.