Koei International, Inc.
Country not established
- Devices
- 1
What Koei International, Inc. makes
Koei International, Inc. manufactures the RECOH ROOT CANAL IRRIGATOR, a Class I medical device.
The company is based in the US and its device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Recoh Root Canal Irrigator Ref K811175
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Koei International, Inc. have in the registry?
The registry currently lists 1 device for Koei International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koei International, Inc.'s devices?
Among its 1 most recently registered device, Koei International, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Koei International, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Koei International, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Koei International, Inc. in the registry?
The most recently registered devices listed for Koei International, Inc. include RECOH ROOT CANAL IRRIGATOR.