Data / Medical devices / Chart, Visual Acuity / United States

FDA-registered makers of Chart, Visual Acuity in the United States: 31 establishments

Name: FDA-registered makers of Chart, Visual Acuity in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

31 establishments in the United States are registered with the FDA to make Chart, Visual Acuity (product code HOX). 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: Chart, Visual Acuity
Product code: HOX
Country: United States

Makers of Chart, Visual Acuity in the United States

Maker	Location	Role	Source
1800 Contacts, Inc	Draper, UT, United States	Manufacturer	api.fda.gov
Adaptive Sensory Technology Inc	San Diego, CA, United States	Manufacturer	api.fda.gov
Ama Optics, Inc.	Miami Beach, FL, United States	Manufacturer	api.fda.gov
Acuity Pro, Inc.	Elk City, OK, United States	Complaint file establishment, Manufacturer	api.fda.gov
Apramed USA LLC	Kissimmee, FL, United States	Manufacturer, Repackager or relabeler	api.fda.gov
Bertec Corp.	Columbus, OH, United States	Manufacturer	api.fda.gov
Eyeque Corporation	Newark, CA, United States	Repackager or relabeler, Specification developer	api.fda.gov
Gobiquity, Inc.	Nashville, TN, United States	Complaint file establishment, Manufacturer, Remanufacturer	api.fda.gov
Gome Optical Lens Company Limited	Yonkers, NY, United States	Manufacturer	api.fda.gov
Good-Lite Co.	Elgin, IL, United States	Manufacturer	api.fda.gov
Gulden Ophthalmics	Elkins Park, PA, United States	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Harvest Digital, LLC	Smithfield, VA, United States	Manufacturer	api.fda.gov
Heru, Inc.	Miami, FL, United States	Complaint file establishment, Manufacturer, Specification developer	api.fda.gov
Lombart Instrument, Inc. d/b/a Marco Ophthalmic	Jacksonville, FL, United States	Specification developer	api.fda.gov
Miller Technical Services	Plymouth, MI, United States	Contract manufacturer	api.fda.gov
Nidek Incorporated	The Colony, TX, United States	Manufacturer	api.fda.gov
Northeastern University	Boston, MA, United States	Specification developer	api.fda.gov
Optego Vision USA, Inc.	Tucson, AZ, United States	Manufacturer	api.fda.gov
Precision Vision	Woodstock, IL, United States	Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler	api.fda.gov
Pursuant Health	Alpharetta, GA, United States	Specification developer	api.fda.gov
Ray Vision Inc.	Lake Forest, CA, United States	Manufacturer	api.fda.gov
Ready Set Import	Beverly Hills, CA, United States	Specification developer	api.fda.gov
Reichert Inc.	Depew, NY, United States	Complaint file establishment, Manufacturer	api.fda.gov
RxSight Inc.	Aliso Viejo, CA, United States	Manufacturer	api.fda.gov
S4optik LLC	Jacksonville, FL, United States	Complaint file establishment, Manufacturer	api.fda.gov
Stereo Optical Company LLC	Chicago, IL, United States	Manufacturer	api.fda.gov
Topcon Healthcare, Inc.	Oakland, NJ, United States	Manufacturer for export	api.fda.gov
Vision Training Products, Inc.	Mishawaka, IN, United States	Repackager or relabeler, Specification developer	api.fda.gov
Vmax Vision Inc.	Longwood, FL, United States	Manufacturer	api.fda.gov
VectorVision Inc.	Greenville, OH, United States	Specification developer	api.fda.gov
Vision Precision Holdings, LLC	Delray Beach, FL, United States	Manufacturer	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.