FDA applicant
Qpix Solutions, Inc.
FDA records 4 decisions for Qpix Solutions, Inc. (Morrisville, NC) from 2023 to 2026: 4 510(k) clearances. All are in product code MUH (System, X-Ray, Extraoral Source, Digital). Since 2016 its 510(k)s took a median of 61 days from receipt to decision, against 144 for FDA’s reviews in the same codes and years. Its devices cite 5 predicates, 4 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Qpix Solutions, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2023.
Planning a device like Qpix Solutions, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report