Ascentia Health Incorporated
Country not established
- Devices
- 1
What Ascentia Health Incorporated makes
Ascentia Health Incorporated makes the Clayton Intra-aural Device (CID).
The Clayton Intra-aural Device (CID) is classified as a Class U device 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
Clayton Intra-Aural Device (Cid) Ref K091880
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ascentia Health Incorporated have in the registry?
The registry currently lists 1 device for Ascentia Health Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ascentia Health Incorporated's devices?
Among its 1 most recently registered device, Ascentia Health Incorporated has devices listed in FDA 510(k) (1 device).
What are the newest devices from Ascentia Health Incorporated in the registry?
The most recently registered devices listed for Ascentia Health Incorporated include CLAYTON INTRA-AURAL DEVICE (CID).