GENESEEQ TECHNOLOGY INC.

FDA Device Registration & Listing · Toronto Ontario, CA · Registration 3043050156

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
3043050156
FEI Number
3043050156
Entity Name
GENESEEQ TECHNOLOGY INC.
City/State/Country
Toronto Ontario, CA
Establishment Address
1802-393 University Ave, Toronto Ontario M5G 1E6, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Geneseeq Technology Inc. (Owner Number: 10094724)
Owner / Operator Contact Address
1802-393 University Ave, Toronto, CA-ON M5G 1E6, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

GENESEEQPRIME NGS Tumor Profiling Assay (FFPE)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PZM Next Generation Sequencing Based Tumor Profiling Test Pathology Class 2 866.6080 2025-12-18

Official Correspondent

Lihua Wang

US Agent Details

Scott Bednar Business: QA/RA CONSULTING GROUP, INC. Email: sbednar@qaraconsultinggroup.com Phone: (412) 4188066

Related Public Records

Same Entity

Geneseeq Technology Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043050156. Last updated year: 2026. Please use registration number 3043050156 when referencing this establishment in official correspondence.
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