Creation North America, Inc.
Country not established
- Devices
- 1
What Creation North America, Inc. makes
Creation North America, Inc. makes the Willi Geller Ceramic Creation & Surprise device.
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
Willi Geller Ceramic Creation & Surprise Ref K900209
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Creation North America, Inc. have in the registry?
The registry currently lists 1 device for Creation North America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Creation North America, Inc.'s devices?
Among its 1 most recently registered device, Creation North America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Creation North America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Creation North America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Creation North America, Inc. in the registry?
The most recently registered devices listed for Creation North America, Inc. include WILLI GELLER CERAMIC CREATION & SURPRISE.