MARIAN CHICAGO, INC.

FDA Device Registration & Listing · West Chicago, IL, US · Registration 3010005578

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
3010005578
FEI Number
3010005578
Entity Name
MARIAN CHICAGO, INC.
City/State/Country
West Chicago, IL, US
Establishment Address
396 Wegner Dr, West Chicago, IL 60185, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Marian Chicago, Inc. (Owner Number: 10094366)
Owner / Operator Contact Address
396 Wegner Dr., West Chicago, IL 60185, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDN System, Perfusion, Kidney Gastroenterology, Urology Class 2 876.5880 2025-11-25

Official Correspondent

Ryan Oakes

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Marian Chicago, Inc.
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
K013575 Organ Recovery Systems, Inc. KPS-I, THE KIDNEY PERFUSION SOLUTION 2002-01-25

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010005578. Last updated year: 2026. Please use registration number 3010005578 when referencing this establishment in official correspondence.
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