Fiberdent Corp.
Country not established
- Devices
- 1
What Fiberdent Corp. makes
Fiberdent Corp. manufactures the ORASCOPE, a dental inspection device designed for intraoral examination and diagnostic imaging.
The ORASCOPE is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Orascope Ref K991011
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fiberdent Corp. have in the registry?
The registry currently lists 1 device for Fiberdent Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fiberdent Corp.'s devices?
Among its 1 most recently registered device, Fiberdent Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Fiberdent Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fiberdent Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fiberdent Corp. in the registry?
The most recently registered devices listed for Fiberdent Corp. include ORASCOPE.