Ako USA, Inc.
Country not established
- Devices
- 1
What Ako USA, Inc. makes
Ako USA, Inc. makes medical devices such as the ULTRA WAVE 101.
The company's portfolio, which includes Class I devices, is listed in the FDA 510k registry and is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ultra Wave 101 Ref K905836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ako USA, Inc. have in the registry?
The registry currently lists 1 device for Ako USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ako USA, Inc.'s devices?
Among its 1 most recently registered device, Ako USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ako USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ako USA, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ako USA, Inc. in the registry?
The most recently registered devices listed for Ako USA, Inc. include ULTRA WAVE 101.