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Data / Medical devices / Fixation, Vision Training, Binocular / United States

FDA-registered makers of Fixation, Vision Training, Binocular in the United States: 5 establishments

5 establishments in the United States are registered with the FDA to make Fixation, Vision Training, Binocular (product code NXR). 0 have 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
Fixation, Vision Training, Binocular
Product code
NXR
Country
United States

Makers of Fixation, Vision Training, Binocular in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Fresnel Prism & Lens Co.Bloomington, MN, United StatesManufacturer0000api.fda.gov
Gulden OphthalmicsElkins Park, PA, United StatesManufacturer0000api.fda.gov
HTS, Inc.Gold Canyon, AZ, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Novavision, Inc.Boca Raton, FL, United StatesManufacturer0000api.fda.gov
Vivid VisionSan Francisco, CA, United StatesSpecification developer0000api.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.