Radworks Corp.
Country not established
- Devices
- 1
What Radworks Corp. makes
Radworks Corp. manufactures the RADWORKS device, a Class II medical device designed for diagnostic or therapeutic use in specific clinical applications.
The RADWORKS device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Radworks Ref K934645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radworks Corp. have in the registry?
The registry currently lists 1 device for Radworks Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radworks Corp.'s devices?
Among its 1 most recently registered device, Radworks Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Radworks Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Radworks Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radworks Corp. in the registry?
The most recently registered devices listed for Radworks Corp. include RADWORKS.