Data / Medical devices / Accessories, Soft Lens Products / United States
FDA-registered makers of Accessories, Soft Lens Products in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Accessories, Soft Lens Products (product code LPN). 9 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
- Accessories, Soft Lens Products
- Product code
- LPN
- Country
- United States
Makers of Accessories, Soft Lens Products 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, Specification developer | 11 | December 6, 2022 | 6 | 3 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Greenville, SC, United States | Manufacturer | 9 | December 6, 2022 | 6 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Fort Worth, TX, United States | Manufacturer, Specification developer | 8 | July 31, 2019 | 0 | 0 | 0 | api.fda.gov |
| Johnson & Johnson Surgical Vision, Inc. | Irvine, CA, United States | Manufacturer, Specification developer | 3 | September 15, 2010 | 3 | 0 | 0 | api.fda.gov |
| Allergan Sales, LLC | Irvine, CA, United States | Complaint file establishment, Specification developer | 2 | August 8, 2019 | 0 | 1 | 0 | api.fda.gov |
| Allergan Sales, LLC | Waco, TX, United States | Manufacturer | 1 | October 7, 1999 | 0 | 0 | 0 | api.fda.gov |
| Altaire Pharmaceuticals, Inc. | Aquebogue, NY, United States | Contract manufacturer, Manufacturer | 1 | April 25, 2007 | 0 | 0 | 0 | api.fda.gov |
| Medtech Products, Inc. | Tarrytown, NY, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| The Lifestyle Co., Inc. | Freehold, NJ, United States | Manufacturer | 1 | May 15, 2020 | 0 | 0 | 0 | api.fda.gov |
| C & J Industries, Inc. | Meadville, PA, United States | Contract manufacturer | 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.