DGNCT LLC

FDA Device Registration & Listing · Miami, FL, US · Registration 3025110425

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
3025110425
FEI Number
3025110425
Entity Name
DGNCT LLC
City/State/Country
Miami, FL, US
Establishment Address
333 Southeast 2nd Avenue, 20th Floor, room 563, Miami, FL 33131, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DGNCT LLC (Owner Number: 10086595)
Owner / Operator Contact Address
333 Southeast 2nd Avenue, 20th Floor, room 563, Miami, FL 33131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Diagnocat Segmentron Viewer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MYN Analyzer, Medical Image Radiology Class 2 892.2070 2026-01-28
QIH Automated Radiological Image Processing Software Radiology Class 2 892.2050 2026-01-28

Official Correspondent

Alex Sanders

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DGNCT LLC
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 3025110425. Last updated year: 2026. Please use registration number 3025110425 when referencing this establishment in official correspondence.
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