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Data / Medical devices / Spectacle, Magnifying / Italy

FDA-registered makers of Spectacle, Magnifying in Italy: 13 establishments

13 establishments in Italy are registered with the FDA to make Spectacle, Magnifying (product code HOI). 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
Spectacle, Magnifying
Product code
HOI
Country
Italy

Makers of Spectacle, Magnifying in Italy

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Key Optical Europe S.R.LScarperia (FI) Firenze, ItalyExporter to the US, Manufacturer0000api.fda.gov
La Giardiniera SRLVENEGONO INFERIORE Varese, ItalyForeign private label distributor, Manufacturer0000api.fda.gov
LUXOTTICA Group SPAAGORDO Belluno, ItalyExporter to the US, Foreign private label distributor, Manufacturer0000api.fda.gov
Luxottica Group S.P.A.Sedico Belluno, ItalyExporter to the US, Foreign private label distributor, Manufacturer0000api.fda.gov
Marcolin SPALONGARONE Belluno, ItalyRepackager or relabeler, Specification developer0000api.fda.gov
MIRAGE S.r.l.VENEGONO SUPERIORE Varese, ItalyManufacturer0000api.fda.gov
Nannini Italian Quality SRLReggio Emilia, ItalyManufacturer0000api.fda.gov
Nau S.P.A.Castiglione Olona Varese, ItalyExporter to the US, Manufacturer0000api.fda.gov
Polinelli S.r.l.Daverio Varese, ItalyManufacturer0000api.fda.gov
Safilo S.P.A.PADOVA Veneto, ItalyContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Sopracolle SRLPERAROLO DI CADORE Belluno, ItalyContract manufacturer0000api.fda.gov
Stilitaly SRLCALALZO DI CADORE Belluno, ItalyContract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Specification developer0000api.fda.gov
Stilo Optical Technology Italy SRLPederobba Treviso, ItalyManufacturer0000api.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.