Data / Medical devices / Lens, Contact (Orthokeratology) / United States
FDA-registered makers of Lens, Contact (Orthokeratology) in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Lens, Contact (Orthokeratology) (product code MUW). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lens, Contact (Orthokeratology)
- Product code
- MUW
- Country
- United States
Makers of Lens, Contact (Orthokeratology) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Contex, Incorporated | Sherman Oaks, CA, United States | Manufacturer | 1 | April 8, 1998 | 0 | 0 | 0 | api.fda.gov |
| Acculens, Inc. | Golden, CO, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Advanced Vision Technologies | Lakewood, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Art Optical Contact Lens, Inc. | Walker, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aurora GP Lab Inc | Goodyear, AZ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bausch & Lomb Incorporated | Wilmington, MA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cler Vision Inc. | Riverside, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hedgefog Research Inc. | San Pedro, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visionary Contact Lens, Inc. | Anaheim, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visionary Optics, LLC | Front Royal, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visionary Optics, LLC | Sterling, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| X-Cel Specialty Contacts | Duluth, GA, 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.