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Data / Medical devices / Frame, Spectacle / United Kingdom

FDA-registered makers of Frame, Spectacle in the United Kingdom: 6 establishments

6 establishments in the United Kingdom 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
United Kingdom

Makers of Frame, Spectacle in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bloobloom LimitedGreater London London, City of, United KingdomExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Cutler And Gross LimitedLondon London, City of, United KingdomManufacturer0000api.fda.gov
FINLAY LondonLondon London, City of, United KingdomSpecification developer0000api.fda.gov
Kimeze Enterprises LimitedNewbury West Berkshire, United KingdomRepackager or relabeler, Specification developer0000api.fda.gov
Luxottica North Europe Ltd.St. Albans, Herts Hertfordshire, United KingdomContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
The Optoplast Actman Eyewear Co LimitedLiverpool, United KingdomExporter to the US, Foreign private label distributor, Manufacturer0000api.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.