RADUX DEVICES INC

FDA Device Registration & Listing · Fridley, MN, US · Registration 3013646819

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
3013646819
FEI Number
3013646819
Entity Name
RADUX DEVICES INC
City/State/Country
Fridley, MN, US
Establishment Address
5201 East River Road, Suite 301, Fridley, MN 55421, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Radux Devices INC (Owner Number: 10055124)
Owner / Operator Contact Address
5201 East River Road, Suite 301, Fridley, MN 55421, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Steradian Shield Steradian Shield

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPY Shield, Protective, Personnel Radiology Class 1 892.6500 2023-10-10
PUI Drape, Surgical, Exempt General, Plastic Surgery Class 2 878.4370 2023-10-10

Official Correspondent

Melinda Swanson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Radux Devices 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 3013646819. Last updated year: 2026. Please use registration number 3013646819 when referencing this establishment in official correspondence.
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