ILMO PRODUCTS COMPANY, INC.

FDA Device Registration & Listing · Jacksonville, IL, US · Registration 1454831

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
1454831
FEI Number
1454831
Entity Name
ILMO PRODUCTS COMPANY, INC.
City/State/Country
Jacksonville, IL, US
Establishment Address
7 Eastgate Drive, Jacksonville, IL 62650, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
ILMO Products Company, Inc. (Owner Number: 10029765)
Owner / Operator Contact Address
7 Eastgate Drive, PO Box 790, Jacksonville, IL 62650, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LASER GAS MIXTURE CLINICAL BLOOD GAS MIXTURES ANAEROBIC MIXTURES LUNG DIFFUSION MIXTURES AEROBIC MIXTURES

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXF Gas, Laser Generating General, Plastic Surgery Class 1 878.4810 2009-06-24
BXK Gas, Calibration (Specified Concentration) Anesthesiology Class 1 868.6400 2009-06-24

Official Correspondent

Kevin Miner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ILMO Products Company, 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 1454831. Last updated year: 2026. Please use registration number 1454831 when referencing this establishment in official correspondence.
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