AMCOR RIGID Packaging USA, LLC

FDA Device Registration & Listing · Fort Worth, TX, US · Registration 3004388281

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
3004388281
FEI Number
3004388281
Entity Name
AMCOR RIGID Packaging USA, LLC
City/State/Country
Fort Worth, TX, US
Establishment Address
4324 FLEETWOOD RD, Fort Worth, TX 76155, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Amcor Rigid Packaging USA, LLC (Owner Number: 10049699)
Owner / Operator Contact Address
10521 S. State Highway M-52, Manchester, MI 48158, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Alcon Contact Lens Case

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2015-07-13

Official Correspondent

Holly Bilinski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Amcor Rigid Packaging USA, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011046360 AMCOR RIGID PACKAGING USA, LLC Millville, NJ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004388281. Last updated year: 2026. Please use registration number 3004388281 when referencing this establishment in official correspondence.
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