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Data / Medical devices / Lens, Condensing, Diagnostic / United States

FDA-registered makers of Lens, Condensing, Diagnostic in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Lens, Condensing, Diagnostic (product code HJL). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Lens, Condensing, Diagnostic
Product code
HJL
Country
United States

Makers of Lens, Condensing, Diagnostic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Atc Technologies Inc.Wilmington, MA, United StatesContract manufacturer0000api.fda.gov
Glaukos CorporationSan Clemente, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Ion Vision, Inc.Campton Hills, IL, United StatesManufacturer0000api.fda.gov
Katena Products, Inc.Parsippany, NJ, United StatesSpecification developer0000api.fda.gov
Katena Products, Inc.Randolph, NJ, United StatesSpecification developer0000api.fda.gov
Ocular Instruments, Inc.Bellevue, WA, United StatesManufacturer0000api.fda.gov
Oculus Surgical IncPort St Lucie, FL, United StatesManufacturer0000api.fda.gov
Volk Optical Inc.Mentor, OH, United StatesManufacturer0010api.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.