Impoaid, Inc.
Country not established
- Devices
- 1
What Impoaid, Inc. makes
Impoaid, Inc. makes the IMPOAID device.
The IMPOAID device is a Class II medical device listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Impoaid Ref K000730
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Impoaid, Inc. have in the registry?
The registry currently lists 1 device for Impoaid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Impoaid, Inc.'s devices?
Among its 1 most recently registered device, Impoaid, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Impoaid, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Impoaid, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Impoaid, Inc. in the registry?
The most recently registered devices listed for Impoaid, Inc. include IMPOAID.