AXIOM MARKETING, INC.

FDA Device Registration & Listing · Green Oaks, IL, US · Registration 3005985361

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
3005985361
FEI Number
3005985361
Entity Name
AXIOM MARKETING, INC.
City/State/Country
Green Oaks, IL, US
Establishment Address
13825 W Business Center Dr, Suite B, Green Oaks, IL 60045, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
AXIOM MARKETING, INC. (Owner Number: 9094026)
Owner / Operator Contact Address
14047 W Petronella Dr, Suite 101, Libertyville, IL 60048, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Aligner Chewies, Retainer Retrievers, Invisible Braces Box Invisalign Aligner Cleaning Foam Invisalign Ultrasonic Cleaning Invisalign Cleaning Crystals + Invisalign Aligner Cleaning Spray Invisalign Cleaning Crystals Invisalign Cleaning System Invisalign; Invisalign Aligner; Invisalign System - Moderate; Invisalign System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ECR Setter, Band, Orthodontic Dental Class 1 872.4565 2026-03-30
EFT Cleanser, Denture, Over The Counter Dental Class 1 872.3520 2024-04-15
NXC Aligner, Sequential Dental Class 2 872.5470 2026-03-30

Official Correspondent

Kathlyn Welch

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AXIOM MARKETING, 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
K902838 Denture Dynamic'S, Inc. DENTURE DYNAMIC'S DENTURE MAGIC 1990-09-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005985361. Last updated year: 2026. Please use registration number 3005985361 when referencing this establishment in official correspondence.
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