GENESIS SOFTWARE INNOVATIONS

FDA Device Registration & Listing · Grand Rapids, MI, US · Registration 3019541896

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
3019541896
FEI Number
3019541896
Entity Name
GENESIS SOFTWARE INNOVATIONS
City/State/Country
Grand Rapids, MI, US
Establishment Address
2851 Charlevoix Dr. SE, Suite 327, Grand Rapids, MI 49546, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Genesis Software Innovations (Owner Number: 10082110)
Owner / Operator Contact Address
2851 Charlevoix Dr. SE, Suite 327, Grand Rapids, MI 49546, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K210556
PMA Number
N/A

All Registered Proprietary Names

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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 2021-06-16

Official Correspondent

Matthew Miller

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Genesis Software Innovations
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 3019541896. Last updated year: 2026. Please use registration number 3019541896 when referencing this establishment in official correspondence.
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