Veraxis Int'L, Inc.
Country not established
- Devices
- 1
What Veraxis Int'L, Inc. makes
Veraxis International, Inc. manufactures the NAKED device, a medical instrument designed for use in specific diagnostic or procedural applications within Class II regulatory classification.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the United States. The manufacturer operates from its base in the US.
Catalogue
Naked Ref K060797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veraxis Int'L, Inc. have in the registry?
The registry currently lists 1 device for Veraxis Int'L, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veraxis Int'L, Inc.'s devices?
Among its 1 most recently registered device, Veraxis Int'L, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Veraxis Int'L, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Veraxis Int'L, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veraxis Int'L, Inc. in the registry?
The most recently registered devices listed for Veraxis Int'L, Inc. include NAKED.