ARxIUM Inc.

FDA Device Registration & Listing · WINNIPEG Manitoba, CA · Registration 3006227536

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
3006227536
FEI Number
3006227536
Entity Name
ARxIUM Inc.
City/State/Country
WINNIPEG Manitoba, CA
Establishment Address
96 NATURE PARK WAY, WINNIPEG Manitoba R3P-0X8, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ARxIUM, Inc. (Owner Number: 9094339)
Owner / Operator Contact Address
1000 Asbury Drive, Suite 4, Buffalo Grove, IL 60089, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RIVA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NEP System/Device, Pharmacy Compounding General Hospital Class 2 880.5440 2006-11-06

Official Correspondent

No official correspondent registered.

US Agent Details

ALAN Schwartz Business: MDI CONSULTANTS Email: info@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012205369 ARxIUM, INC. Buffalo Grove, IL, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006227536. Last updated year: 2026. Please use registration number 3006227536 when referencing this establishment in official correspondence.
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