Vios Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Vios Medical, Inc. makes
Vios Medical, Inc. manufactures patient monitoring systems, including hardware like the Vios Monitoring System Model 2050, and associated software solutions such as the Vios Central Station Monitor and Vios Central Server Software. These products are designed for real-time patient vital sign monitoring in clinical environments.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Vios Monitoring System Ref K150992
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Vios Monitoring System™ Model 2050 Ref K172586
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vios Medical, Inc. have in the registry?
The registry currently lists 3 devices for Vios Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vios Medical, Inc.'s devices?
Among its 3 most recently registered devices, Vios Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vios Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vios Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vios Medical, Inc. in the registry?
The most recently registered devices listed for Vios Medical, Inc. include Vios Monitoring System, Vios Central Station Monitor Software, Vios Central Server Software and Vios Monitoring System™ Model 2050.