Data / Medical devices / Digital Visual Acuity Test / United States
FDA-registered makers of Digital Visual Acuity Test in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make Digital Visual Acuity Test (product code QTO). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Digital Visual Acuity Test
- Product code
- QTO
- Country
- United States
Makers of Digital Visual Acuity Test in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 123 See | Boston, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| 1800 Contacts, Inc | Draper, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Adaptive Sensory Technology Inc | San Diego, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ama Optics, Inc. | Miami Beach, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ckvulpeculae, LLC | San Diego, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diagnosys LLC | Lowell, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eyecheq, Inc | Miami, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eyeque Corporation | Newark, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gome Optical Lens Company Limited | Yonkers, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hedgefog Research Inc. | San Pedro, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heru, Inc. | Miami, FL, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KYS Vision, Inc. | Elko, NV, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M&S Technologies | Niles, IL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M&S Technologies | Thayne, WY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medneuroptek Inc. | Johns Creek, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micro Medical Devices, Inc. | Calabasas, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visibly | Wilmington, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Warby Parker | New York, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| eyeMobil Innovations | Benton Harbor, MI, 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.