Biogenix, Inc.
Country not established
- Devices
- 1
What Biogenix, Inc. makes
Biogenix, Inc. manufactures the Cardiorhythm 2000, a device designed for monitoring and managing cardiac rhythm disorders, including arrhythmias.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
Cardiorhythm 2000 Ref K841472
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biogenix, Inc. have in the registry?
The registry currently lists 1 device for Biogenix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biogenix, Inc.'s devices?
Among its 1 most recently registered device, Biogenix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biogenix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biogenix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biogenix, Inc. in the registry?
The most recently registered devices listed for Biogenix, Inc. include CARDIORHYTHM 2000.