Qt Imaging, Inc.
United Statesfrom the FDA registration address FDA FEI 3011599810
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
QT Scanner 2000 Model A Ref K220933
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011599810
- DUNS number
- 035528118
- Address
- 3 Hamilton Landing, Novato, CA, 94949
Frequently asked questions
How many devices does Qt Imaging, Inc. have in the registry?
The registry currently lists 3 devices for Qt Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Qt Imaging, Inc.'s devices?
Among its 3 most recently registered devices, Qt Imaging, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Qt Imaging, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Qt Imaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Qt Imaging, Inc. in the registry?
The most recently registered devices listed for Qt Imaging, Inc. include QT Scanner 2000 Model B, QT Scanner 2000 and QT Scanner 2000 Model A.