Connexall USA, Inc.
Country not established
- Devices
- 1
What Connexall USA, Inc. makes
Connexall USA, Inc. develops a suite of software products designed for medical device connectivity and data integration, facilitating interoperability between clinical systems and devices.
The portfolio is regulated as Class II devices under FDA 510(k) clearance requirements and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Connexall Suite Of Software Products Ref K112650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Connexall USA, Inc. have in the registry?
The registry currently lists 1 device for Connexall USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Connexall USA, Inc.'s devices?
Among its 1 most recently registered device, Connexall USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Connexall USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Connexall USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Connexall USA, Inc. in the registry?
The most recently registered devices listed for Connexall USA, Inc. include CONNEXALL SUITE OF SOFTWARE PRODUCTS.