Data / Medical devices / Case, Contact Lens / United States
FDA-registered makers of Case, Contact Lens in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Case, Contact Lens (product code LRX). 12 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Case, Contact Lens
- Product code
- LRX
- Country
- United States
Makers of Case, Contact Lens in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Nomax, Inc. | Affton, MO, United States | Contract manufacturer, Repackager or relabeler, Specification developer | 2 | June 6, 2000 | 0 | 0 | 0 | api.fda.gov |
| Apothecary Products, LLC. | Burnsville, MN, United States | Repackager or relabeler, Specification developer | 1 | July 14, 2011 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 1 | January 20, 1998 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 1 | November 20, 2001 | 0 | 0 | 0 | api.fda.gov |
| Fourth Axis LLC | Boise, ID, United States | Specification developer | 1 | February 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| ICU Eyecare Solutions Inc. | Hollister, CA, United States | Specification developer | 1 | June 6, 2000 | 0 | 0 | 0 | api.fda.gov |
| Novabay Pharmaceuticals, Inc | Emeryville, CA, United States | Manufacturer | 1 | April 29, 2015 | 0 | 0 | 0 | api.fda.gov |
| Optego Vision USA, Inc. | Tucson, AZ, United States | Manufacturer | 1 | December 5, 2011 | 0 | 0 | 0 | api.fda.gov |
| Pro-Optics LLC | Palatine, IL, United States | Manufacturer, Repackager or relabeler | 1 | February 9, 1988 | 0 | 0 | 0 | api.fda.gov |
| Paragon Vision Sciences, Inc. | Gilbert, AZ, United States | Complaint file establishment, Manufacturer | 1 | June 12, 2003 | 0 | 0 | 0 | api.fda.gov |
| Tworoger Associates, Ltd. | New York, NY, United States | Specification developer | 1 | June 6, 2000 | 0 | 0 | 0 | api.fda.gov |
| The Hilsinger Company Parent, LLC | Mansfield, MA, United States | Complaint file establishment, Specification developer | 1 | January 25, 2005 | 0 | 0 | 0 | api.fda.gov |
| Amcor Rigid Packaging Solutions International | Brookville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amcor Rigid Packaging Usa, LLC | Millville, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alltrista Plastics LLC | Greer, SC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lighthouse Tech | Chandler, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R.E.C. Manufacturing Corporation | Hopedale, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.