Data / Medical devices / United States / Qpix Solutions, Inc.
Qpix Solutions, Inc.: FDA-registered device maker in Morrisville, NC, United States, 1 510(k) clearance
Qpix Solutions, Inc. is registered with the FDA (registration 3042046320) in Morrisville, NC, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 10, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042046320
- Address
- 1001 Aviation Parkway Suite 200, Morrisville, NC, United States, 27560
- Owner or operator
- QPIX SOLUTIONS, INC. (10086838)
- Roles
- Manufacturer
- First device listed
- April 22, 2026
- Registered through
- 2026
- Brand names listed
- EzSensor HD (IOS-U20IF, IOS-U15IF, IOS-U10IF), X Sensor UHD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, X-Ray, Extraoral Source, Digital | MUH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 10, 2025 | K252570 | EzSensor HD, EzSensor UHD | MUH | Substantially Equivalent | Qpix Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 10, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.