Aon Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Aon Co., Ltd. makes
Aon Co., Ltd. makes the INNI-CERA device.
The INNI-CERA device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Inni-Cera Ref K211308
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aon Co., Ltd. have in the registry?
The registry currently lists 1 device for Aon Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aon Co., Ltd.'s devices?
Among its 1 most recently registered device, Aon Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Aon Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aon Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aon Co., Ltd. in the registry?
The most recently registered devices listed for Aon Co., Ltd. include INNI-CERA.