Affix Medical - mHUB Facility

FDA Device Registration & Listing · Chicago, IL, US · Registration 3043354155

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
3043354155
FEI Number
3043354155
Entity Name
Affix Medical - mHUB Facility
City/State/Country
Chicago, IL, US
Establishment Address
1623 W Fulton St, Chicago, IL 60612, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Affix Medical (Owner Number: 10095287)
Owner / Operator Contact Address
1623 W Fulton St, Chicago, IL 60612, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Affix Clip

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2026-02-18

Official Correspondent

Christopher Wilson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Affix Medical
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 3043354155. Last updated year: 2026. Please use registration number 3043354155 when referencing this establishment in official correspondence.
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