Fairy World, Inc.
Country not established
- Devices
- 1
What Fairy World, Inc. makes
Fairy World, Inc. manufactures Class I medical devices, including products such as the FAIRY WORLD INC device, which are intended for low-risk applications.
These devices are regulated under the FDA’s 510(k) pathway and are listed in the U.S. regulatory system. The company is based in the United States.
Catalogue
Fairy World Inc Ref K951992
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fairy World, Inc. have in the registry?
The registry currently lists 1 device for Fairy World, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fairy World, Inc.'s devices?
Among its 1 most recently registered device, Fairy World, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fairy World, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fairy World, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fairy World, Inc. in the registry?
The most recently registered devices listed for Fairy World, Inc. include FAIRY WORLD INC.