Data / Medical devices / Products, Contact Lens Care, Rigid Gas Permeable / United States
FDA-registered makers of Products, Contact Lens Care, Rigid Gas Permeable in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Products, Contact Lens Care, Rigid Gas Permeable (product code MRC). 3 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
- Products, Contact Lens Care, Rigid Gas Permeable
- Product code
- MRC
- Country
- United States
Makers of Products, Contact Lens Care, Rigid Gas Permeable 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 | 7 | September 23, 2020 | 0 | 1 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Greenville, SC, United States | Manufacturer | 5 | August 10, 2018 | 0 | 0 | 0 | api.fda.gov |
| Dry Eye Innovations, LLC | Franklin, TN, United States | Specification developer | 1 | July 31, 2020 | 0 | 0 | 0 | api.fda.gov |
| Allergan Sales, LLC | Irvine, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Altaire Pharmaceuticals, Inc. | Aquebogue, NY, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Fort Worth, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ClensTech Inc.dba ASEPT PAK INC. | Malone, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Lifestyle Co., Inc. | Freehold, NJ, 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.