Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Italy
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Italy: 15 establishments
15 establishments in Italy are registered with the FDA to make Lens, Spectacle, Non-Custom (Prescription) (product code HQG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- Italy
Makers of Lens, Spectacle, Non-Custom (Prescription) in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Asg International SRL | MUSSOLENTE Vicenza, Italy | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Atmosphera SRL | PEDEROBBA Treviso, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Barberini S.P.A. | Silvi Teramo, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Vision Italia S.P.A. | CASTIGLIONE OLONA Varese, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| De Lotto S.R.L. | SAN VITO DI CADORE Belluno, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Divel Italia SPA | Calderara di Reno (BO) Emilia-Romagna, Italy | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| La Fabbrica S.R.L. | SETTEVILLE Belluno, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| La Giardiniera SRL | VENEGONO INFERIORE Varese, Italy | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lud'o SRL | Milan Milano, Italy | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luxol SRL | LOZZO DI CADORE Belluno, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LUXOTTICA Group SPA | AGORDO Belluno, Italy | Exporter to the US, Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luxottica Group S.P.A. | Sedico Belluno, Italy | Exporter to the US, Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MIRAGE S.r.l. | VENEGONO SUPERIORE Varese, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Polinelli S.r.l. | Daverio Varese, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stilitaly SRL | CALALZO DI CADORE Belluno, Italy | Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Specification developer | 0 | 0 | 0 | 0 | api.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.