Koning Corporation
Country not established FDA FEI 3008513054
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
- GUDID
Koning Breast CT, KBCT Ref P130025
PMA PMA
Company details
- FDA FEI number
- 3008513054
- DUNS number
- 145060716
- Address
- 5555 Oakbrook Pkwy Ste 640, Norcross, GA, 30093
- [email protected]
- Phone
- 678-481-9246
Frequently asked questions
How many devices does Koning Corporation have in the registry?
The registry currently lists 3 devices for Koning Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koning Corporation's devices?
Among its 3 most recently registered devices, Koning Corporation has devices listed in FDA PMA (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 Koning Corporation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Koning Corporation's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Koning Corporation in the registry?
The most recently registered devices listed for Koning Corporation include Koning Breast CT System CBCT 1000 and Koning Breast CT, KBCT.