510(k) Report

FDA applicant

UAB Ligence

Kaunas, LT1 decision2026–20260 recalls

FDA records 1 decision for UAB Ligence (Kaunas, LT) in 2026: 1 510(k) clearance. All are in product code QIH (Automated Radiological Image Processing Software). No recall is linked to its devices.

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 UAB Ligence’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026 (partial year): 1
2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

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Which product codes does it file in?

  • QIHAutomated Radiological Image Processing Software1decision

What has FDA decided for it lately?

  • K261733Ligence HeartUAB Ligence · 2026

The one decision as UAB Ligence →