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Data / Medical devices / Frame, Spectacle / Germany

FDA-registered makers of Frame, Spectacle in Germany: 19 establishments

19 establishments in Germany are registered with the FDA to make Frame, Spectacle (product code HQZ). 1 has 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
Germany

Makers of Frame, Spectacle in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
LUNOR AktiengesellschaftBad Liebenzell Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer1December 8, 1993000api.fda.gov
A. Schweizer GMBHFORCHHEIM Bavaria, GermanyExporter to the US, Manufacturer0000api.fda.gov
Additive Scale GMBHKrailling Bavaria, GermanyManufacturer0000api.fda.gov
Carl Zeiss Vision GMBHAALEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
DR. EUGEN BECK GmbH & Co. FLAIRPassau Bavaria, GermanyManufacturer0000api.fda.gov
Fielmann Group AGHamburg, GermanySpecification developer0000api.fda.gov
Ivko GMBHNITZ Rhineland-Palatinate, GermanyManufacturer0000api.fda.gov
Lotos Goldbrillen GMBHEisingen Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Maybach Icons Of Luxury GMBHBaar Rhineland-Palatinate, GermanyManufacturer0000api.fda.gov
Mykita GMBHberlin, GermanyManufacturer0000api.fda.gov
Op Couture Brillen GMBHPASSAU Bavaria, GermanyManufacturer, Specification developer0000api.fda.gov
OWP Brillen GmbHPassau Bavaria, GermanyManufacturer0000api.fda.gov
PM Frost GMBH - Eyewear & AccessoriesSASBACH Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Rodenstock GmbHMunich Bavaria, GermanyForeign private label distributor, Specification developer0000api.fda.gov
SchnuchelHolm Schleswig-Holstein, GermanyManufacturer0000api.fda.gov
Walter Wissing & Co. Inh. Olaf LauerBensheim Hesse, GermanyManufacturer0000api.fda.gov
Weareannu GMBHNuremberg Bavaria, GermanyManufacturer0000api.fda.gov
Zettner Brillenfabrikation GMBHFurth Bavaria, GermanyManufacturer0000api.fda.gov
ic! berlin GmbHBerlin, GermanyManufacturer0000api.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.