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Data / Medical devices / Frame, Spectacle / Belgium

FDA-registered makers of Frame, Spectacle in Belgium: 5 establishments

5 establishments in Belgium are registered with the FDA to make Frame, Spectacle (product code HQZ). 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, Spectacle
Product code
HQZ
Country
Belgium

Makers of Frame, Spectacle in Belgium

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Eye Specials InternationalMOL Antwerpen, BelgiumContract manufacturer, Exporter to the US0000api.fda.gov
HenauKORTRIJK West-Vlaanderen, BelgiumSpecification developer0000api.fda.gov
Hoet Eyewear Design BVBrugge Brussels-Capital Region, BelgiumExporter to the US, Manufacturer0000api.fda.gov
Matthieu Duchene DesignBruxelles Brussels-Capital Region, BelgiumExporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Theo BVANTWERP Antwerpen, BelgiumManufacturer0000api.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.