Q Bio, Inc.
Country not established
- Devices
- 2
What Q Bio, Inc. makes
Q Bio, Inc. manufactures the Constellation (CON-001), a medical device designed for [specific application not provided in data]. This product falls under the category of [unspecified category], addressing [functional purpose not detailed in data].
The Constellation device is classified as a Class II product under FDA regulations and has been authorised through the 510(k) clearance pathway. The company is based in the United States.
Catalogue
- GUDID
Constellation (CON-001) Ref K241280
510(k) 510(k)
Company details
- DUNS number
- 080344353
- [email protected]
- Phone
- 9999999999
Frequently asked questions
How many devices does Q Bio, Inc. have in the registry?
The registry currently lists 2 devices for Q Bio, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Q Bio, Inc.'s devices?
Among its 2 most recently registered devices, Q Bio, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Q Bio, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Q Bio, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Q Bio, Inc. in the registry?
The most recently registered devices listed for Q Bio, Inc. include Constellation SW004 and Constellation (CON-001).