Data / Medical devices / Lens, Intraocular, Toric Optics / United States
FDA-registered makers of Lens, Intraocular, Toric Optics in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Lens, Intraocular, Toric Optics (product code MJP). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lens, Intraocular, Toric Optics
- Product code
- MJP
- Country
- United States
Makers of Lens, Intraocular, Toric Optics in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Amo Puerto Rico Manufacturing, Inc | Anasco, PR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Huntington, WV, United States | Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Lesage, WV, United States | Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Wilmington, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Clearwater, FL, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Johnson & Johnson Surgical Vision, Inc. | Irvine, CA, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Millennium Biomedical, Inc. | Pomona, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Staar Surgical Company | Monrovia, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STAAR Surgical Company | Tustin, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.