FDA applicant

Qubyx Limited

Nice, FR3 decisions2012–20150 recalls

FDA records 3 decisions for Qubyx Limited (Nice, FR) from 2012 to 2015: 3 510(k) clearances. Most are in product codes PGY (Display, Diagnostic Radiology) and LLZ (System, Image Processing, Radiological). Its devices cite 4 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Qubyx , Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Qubyx Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Qubyx Limited by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Qubyx Limited’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Qubyx”

FDA records each applicant name separately; these may or may not be the same firm.

Qubyx Software Technologies, Inc. 2

Qubyx Limited

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Qubyx”