Data / Medical devices / Lenses, Soft Contact, Extended Wear / United States
FDA-registered makers of Lenses, Soft Contact, Extended Wear in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Lenses, Soft Contact, Extended Wear (product code LPM). 9 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lenses, Soft Contact, Extended Wear
- Product code
- LPM
- Country
- United States
Makers of Lenses, Soft Contact, Extended Wear in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bausch & Lomb Incorporated | Rochester, NY, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 5 | 1 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Lynchburg, VA, United States | Manufacturer | 0 | 5 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Duluth, GA, United States | Repackager or relabeler, Specification developer | 0 | 2 | 5 | 0 | api.fda.gov | |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 0 | 2 | 0 | 0 | api.fda.gov | |
| COOPERVISION Manufacturing Puerto Rico, LLC | Juana Diaz, PR, United States | Complaint file establishment, Manufacturer | 0 | 2 | 1 | 0 | api.fda.gov | |
| Coopervision, Inc. | Scottsville, NY, United States | Complaint file establishment, Manufacturer | 0 | 2 | 1 | 0 | api.fda.gov | |
| Johnson & Johnson Vision Care, Inc. | Jacksonville, FL, United States | Manufacturer | 0 | 2 | 2 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Clearwater, FL, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Kontur Kontact Lens Co., Inc. | Hercules, CA, United States | Manufacturer | 0 | 1 | 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.