Qpix Solutions, Inc.
Country not established FDA establishment FEI 3025442726
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
EzSensor HD Ref K261663
510(k) 510(k)EzSensor HD, EzSensor UHD Ref K252570
510(k) 510(k)EZSensor XHD Ref K232255
510(k) 510(k)X Sensor (Model: IOS-A15IF, HDI-15DGF) Ref K242778
510(k) 510(k)
Company details
- FDA FEI number
- 3025442726
- Address
- 2933 S Miami Blvd Ste 119, Durham, Durham, NC, 27703
Frequently asked questions
How many devices does QPIX SOLUTIONS, INC. have in the registry?
The registry currently lists 4 devices for QPIX SOLUTIONS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list QPIX SOLUTIONS, INC.'s devices?
Among its 4 most recently registered devices, QPIX SOLUTIONS, INC. has devices listed in FDA 510(k) (4 devices).
What risk classes do QPIX SOLUTIONS, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for QPIX SOLUTIONS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from QPIX SOLUTIONS, INC. in the registry?
The most recently registered devices listed for QPIX SOLUTIONS, INC. include EzSensor HD, EzSensor HD, EzSensor UHD, EZSensor XHD and X Sensor (Model: IOS-A15IF, HDI-15DGF).