Veresure, Inc.
Country not established
- Devices
- 1
What Veresure, Inc. makes
Veresure, Inc. manufactures the Veresure Bell, a medical device designed for auditory signaling in clinical or patient care settings.
The Veresure Bell is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Veresure Bell Ref K061387
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veresure, Inc. have in the registry?
The registry currently lists 1 device for Veresure, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veresure, Inc.'s devices?
Among its 1 most recently registered device, Veresure, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Veresure, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Veresure, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veresure, Inc. in the registry?
The most recently registered devices listed for Veresure, Inc. include VERESURE BELL.