Vault Paragon Group, Inc.
Country not established FDA establishment FEI 3018681450
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
VaporShield Ref K250847
510(k) 510(k)PowerPAK Syringe Ref K220114
510(k) 510(k)
Company details
- FDA FEI number
- 3018681450
- Address
- 199 E 52nd Street, Garden City, ID, 83714
Frequently asked questions
How many devices does VAULT PARAGON GROUP, INC. have in the registry?
The registry currently lists 4 devices for VAULT PARAGON GROUP, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VAULT PARAGON GROUP, INC.'s devices?
Among its 4 most recently registered devices, VAULT PARAGON GROUP, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do VAULT PARAGON GROUP, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for VAULT PARAGON GROUP, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from VAULT PARAGON GROUP, INC. in the registry?
The most recently registered devices listed for VAULT PARAGON GROUP, INC. include OCCIGUIDE ER 1000, Zephyrus Innovations ZE-010, VaporShield and PowerPAK Syringe.