Raypia Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Raypia Co., Ltd. makes
Raypia Co., Ltd. manufactures the Rextar Pro, which is a portable dental X-ray system.
This device 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
Rextar Pro Ref K242185
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Raypia Co., Ltd. have in the registry?
The registry currently lists 1 device for Raypia Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Raypia Co., Ltd.'s devices?
Among its 1 most recently registered device, Raypia Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Raypia Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Raypia Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Raypia Co., Ltd. in the registry?
The most recently registered devices listed for Raypia Co., Ltd. include Rextar Pro.