Denfotex Light Systems, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Denfotex Light Systems, Ltd. makes
Denfotex Light Systems, Ltd. manufactures the SAVEDENT BLUE, which is a dental light system.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Savedent Blue Ref K042196
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Denfotex Light Systems, Ltd. have in the registry?
The registry currently lists 1 device for Denfotex Light Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Denfotex Light Systems, Ltd.'s devices?
Among its 1 most recently registered device, Denfotex Light Systems, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Denfotex Light Systems, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Denfotex Light Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Denfotex Light Systems, Ltd. in the registry?
The most recently registered devices listed for Denfotex Light Systems, Ltd. include SAVEDENT BLUE.