Viox Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Viox Corp. makes
Viox Corp. manufactures lead glass shields for radiation protection and the Duffy Bolus Injector, a device used to administer bolus fluids in medical procedures.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. Viox Corp. is based in the United States.
Catalogue
Lead Glass Shields Ref K872656
Regimes: 510(k) Registry: 510(k)Duffy Bolus Injector Ref K863936
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viox Corp. have in the registry?
The registry currently lists 2 devices for Viox Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viox Corp.'s devices?
Among its 2 most recently registered devices, Viox Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Viox Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Viox Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Viox Corp. in the registry?
The most recently registered devices listed for Viox Corp. include LEAD GLASS SHIELDS and DUFFY BOLUS INJECTOR.