Cozcon, Inc.
Country not established
- Devices
- 1
What Cozcon, Inc. makes
Cozcon, Inc. manufactures REFLUX BED devices, which are designed for patient positioning and support in medical settings.
The REFLUX BED falls under FDA Class I regulation and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Reflux Bed Ref K896256
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cozcon, Inc. have in the registry?
The registry currently lists 1 device for Cozcon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cozcon, Inc.'s devices?
Among its 1 most recently registered device, Cozcon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cozcon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cozcon, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cozcon, Inc. in the registry?
The most recently registered devices listed for Cozcon, Inc. include REFLUX BED.