Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008434737

FEI Number

3005651716

Entity Name

EUROFINS VIRACOR, LLC

City/State/Country

Lenexa, KS, US

Establishment Address

18000 W 99th Street, Suite 10, Lenexa, KS 66219, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Eurofins Viracor (Owner Number: 10043353)

Owner / Operator Contact Address

18000 W 99th Street, Suite 10, Lenexa, KS 66219, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K013169

PMA Number

N/A

All Registered Proprietary Names

Immuknow

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NID	Assay, Proliferation, In Vitro, T Lymphocyte	Hematology	Class 2	864.5220	2013-02-07

Official Correspondent

Christina Gonzalez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Eurofins Viracor

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 3008434737. Last updated year: 2026. Please use registration number 3008434737 when referencing this establishment in official correspondence.