Data / Medical devices / United States / Global Packaging Systems Inc
Global Packaging Systems Inc: FDA-registered device maker in Fort Worth, TX, United States, 8 510(k) clearances
Global Packaging Systems Inc is registered with the FDA (registration 3003306559) in Fort Worth, TX, United States. It lists 3 device types. The FDA files 8 510(k) clearances under its listings, the newest dated January 26, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003306559
- Address
- 3001 Northern Cross BLVD Ste 361, Fort Worth, TX, United States, 76137
- Owner or operator
- Global Packaging Systems Inc (10047081)
- Roles
- Repackager or relabeler
- First device listed
- June 25, 2014
- Registered through
- 2026
- Brand names listed
- LPN, LRX, MRC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Soft Lens Products | LPN | 2 | Repackager or relabeler | accessdata.fda.gov |
| Case, Contact Lens | LRX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Products, Contact Lens Care, Rigid Gas Permeable | MRC | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 26, 2015 | K142284 | CLEAR CARE PLUS CLEANING & DISINFECTIONG SOLUTION WITH HYDRAGLYDE | LPN | Substantially Equivalent | Alcon Laboratories, Inc. | accessdata.fda.gov |
| May 10, 2011 | K102860 | ALCON MULTI-PIRPOSE DISINFECTING SOLUTION | LPN | Substantially Equivalent | Alcon Research, Ltd. | accessdata.fda.gov |
| September 14, 2005 | K050729 | ALCON MULTI-PURPOSE DISINFECTING SOLUTION | LPN | Substantially Equivalent | Alcon Research, Ltd. | accessdata.fda.gov |
| June 27, 2003 | K031521 | AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION | LPN | Substantially Equivalent | Ciba Vision Corporation | accessdata.fda.gov |
| January 14, 1999 | K984575 | MULTI-PURPOSE DISINFECTING SOLUTION ID 90746 | LPN | Substantially Equivalent | Alcon Laboratories | accessdata.fda.gov |
| January 20, 1998 | K974281 | ALCON CONTACT LENS CASE | LRX | Substantially Equivalent | Alcon Laboratories | accessdata.fda.gov |
| July 14, 1997 | K971618 | ALCON CONTACT LENS CASE | LRX | Substantially Equivalent | Alcon Laboratories | accessdata.fda.gov |
| June 28, 1993 | K931620 | OPTI-FREE CONTACT LENS CASE | LRX | Substantially Equivalent | Alcon Laboratories | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Soft Lens Products
- All makers of Products, Contact Lens Care, Rigid Gas Permeable
- All makers of Case, Contact Lens
Updated January 26, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.