GLOBAL PACKAGING SYSTEMS INC

FDA Device Registration & Listing · Fort Worth, TX, US · Registration 3003306559

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
3003306559
FEI Number
3003306559
Entity Name
GLOBAL PACKAGING SYSTEMS INC
City/State/Country
Fort Worth, TX, US
Establishment Address
3001 NORTHERN CROSS BLVD STE 361, Fort Worth, TX 76137, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Global Packaging Systems Inc (Owner Number: 10047081)
Owner / Operator Contact Address
3001 Northern Cross, Ste 361, Fort Worth, TX 76137, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

LPN MRC LPN LRX LRX LPN LPN

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRC Products, Contact Lens Care, Rigid Gas Permeable Ophthalmic Class 2 886.5918 2015-11-16
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2015-11-16
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2014-06-25
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2015-11-16
LRX Case, Contact Lens Ophthalmic Class 2 886.5928 2015-11-16
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2014-06-25
LPN Accessories, Soft Lens Products Ophthalmic Class 2 886.5928 2014-06-25

Official Correspondent

Cindy Musser

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Global Packaging Systems 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
K093254 Abbott Medical Optics, Inc. AMO BRAND MULTI-PURPOSE DISINFECTING SOLUTION 2010-09-15

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0030-2022 Contamac Solutions, Inc. 2
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002
Z-0028-05 Ciba Vision Corporation 2
SOLO-care Plus with Aqualube, Multi-purpose solution*** AquaSoft (Private label), Multi-purpose solution***Sterile***For soft lenses, CIBA Vision Corporation, Made in Canada, Assembled in Canada, Manufactured for: CIBA Vision Corporation, Duluth, GA 30097 USA. The product is distributed in units of single or twin packs containing 2 to 12 ounces of product.
Z-0129-2011 Abbott Medical Optics Inc (AMO) 2
AMO COMPLETE Multi-Purpose Solution, Formula: 9424x; Product Code: 93504 (360ml), 93505 (2x 360ml duo pack), 93515 (240 ml). Cleans, rinses, disinfects, and stores all soft contact lenses and helps keep your eyes protected from dryness and irritation throughout the day.
Z-0130-2011 Abbott Medical Optics Inc (AMO) 2
AMO Total Care (1) Contact Lens Solution, Formula: 8772x; Product Code: 90275 (240 ml). Relieves the dryness, irritation, and discomfort that may be associated with contact lens wear.

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1313525 Bausch & Lomb Incorporated Rochester, NY, US
3004178847 AMO (HANGZHOU) CO., LTD. HANGZHOU Zhejiang, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003306559. Last updated year: 2026. Please use registration number 3003306559 when referencing this establishment in official correspondence.
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