Data / Medical devices / Lens, Contact, (Disposable) / United States
FDA-registered makers of Lens, Contact, (Disposable) in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Lens, Contact, (Disposable) (product code MVN). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Lens, Contact, (Disposable)
- Product code
- MVN
- Country
- United States
Makers of Lens, Contact, (Disposable) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alcon Research, LLC | Duluth, GA, United States | Manufacturer, Repackager or relabeler, Specification developer | 4 | September 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 4 | September 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Manufacturer, Specification developer | 3 | October 25, 2011 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Lynchburg, VA, United States | Manufacturer | 2 | June 10, 2008 | 0 | 0 | 0 | api.fda.gov |
| COOPERVISION Manufacturing Puerto Rico, LLC | Juana Diaz, PR, United States | Complaint file establishment, Manufacturer | 1 | November 22, 2006 | 0 | 0 | 0 | api.fda.gov |
| Johnson & Johnson Vision Care, Inc. | Jacksonville, FL, United States | Complaint file establishment, Manufacturer | 1 | August 12, 2005 | 0 | 3 | 0 | api.fda.gov |
| Coopervision, Inc. | Scottsville, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meti Optical Inc | Dover, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| TANGIBLE SCIENCE Inc | Campbell, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visioneering Technologies, Inc | Alpharetta, GA, United States | 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.