Cleared Traditional

Ligence Heart

K253535 · Ligence Uab · Radiology

Feb 2026

Decision

106d

Days

Class 2

Risk

About This 510(k) Submission

K253535 is an FDA 510(k) clearance for the Ligence Heart, a Automated Radiological Image Processing Software (Class II — Special Controls, product code QIH), submitted by Ligence Uab (Kaunas, LT). The FDA issued a Cleared decision on February 27, 2026, 106 days after receiving the submission on November 13, 2025. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number	K253535 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 13, 2025
Decision Date	February 27, 2026
Days to Decision	106 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Statement

Device Classification

Product Code	QIH — Automated Radiological Image Processing Software
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 892.2050
Definition	To Provide Automated Radiological Image Processing And Analysis Tools. Software Implementing Artificial Intelligence Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Data. In These Devices, The Algorithm Training Data Typically Impacts Device Performance. Adaptive Ai Algorithms Are Not Within Scope Of This Product Code.