"UAB" Ligence

FDA Device Registration & Listing · Kaunas, LT · Registration 3042955884

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3042955884
FEI Number
3042955884
Entity Name
"UAB" Ligence
City/State/Country
Kaunas, LT
Establishment Address
Taikos pr. 54, Kaunas 51305, LT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
UAB "Ligence" (Owner Number: 10094858)
Owner / Operator Contact Address
Taikos pr. 54, Kaunas, LT-16 51305, LT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Ligence Heart

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2025-12-30

Official Correspondent

Alvaro Perez Moreno

US Agent Details

Benzy Arazy Business: Medes USA C/O Matan Arazy Email: Medes@Arazygroup.com Phone: (415) 9921126

Related Public Records

Same Entity

UAB "Ligence"
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K242270 Orthofix Srl OrthoNext Platform System 2024-12-19
K261713 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.6.0) 2026-06-18
K243647 FUJIFILM Healthcare Americas Corporation Synapse PACS (7.5) 2025-06-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042955884. Last updated year: 2026. Please use registration number 3042955884 when referencing this establishment in official correspondence.
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