AEROSOL AND LIQUID PACKAGING

FDA Device Registration & Listing · Baltimore, MD, US · Registration 1120890

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
1120890
FEI Number
1120890
Entity Name
AEROSOL AND LIQUID PACKAGING
City/State/Country
Baltimore, MD, US
Establishment Address
3701 A Southwestern Blvd, Baltimore, MD 21229, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Aerosol and Liquid Packaging (Owner Number: 10080204)
Owner / Operator Contact Address
3701 A Southwestern Blvd, Baltimore, MD 21229, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BC3 Technologies

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2021-01-19

Official Correspondent

Wayne Grube

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aerosol and Liquid Packaging
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1120890. Last updated year: 2026. Please use registration number 1120890 when referencing this establishment in official correspondence.
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