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Data / Medical devices / Frame, Trial, Ophthalmic / United States

FDA-registered makers of Frame, Trial, Ophthalmic in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Frame, Trial, Ophthalmic (product code HPA). 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
Frame, Trial, Ophthalmic
Product code
HPA
Country
United States

Makers of Frame, Trial, Ophthalmic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ama Optics, Inc.Miami Beach, FL, United StatesManufacturer0000api.fda.gov
Alcon Research, LLCDuluth, GA, United StatesSpecification developer0000api.fda.gov
Elevate Solutions Group, LLCAustell, GA, United StatesContract manufacturer0000api.fda.gov
Eyeque CorporationNewark, CA, United StatesManufacturer, Remanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Gulden OphthalmicsElkins Park, PA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Precision VisionWoodstock, IL, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
Ray Vision Inc.Lake Forest, CA, United StatesRepackager or relabeler, Specification developer0000api.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.