Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / France
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in France: 9 establishments
9 establishments in France 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 2, 2026.
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- Device
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- France
Makers of Lens, Spectacle, Non-Custom (Prescription) in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BBGR | SEZANNE Marne, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BNL Eurolens SA | MONTANGES Ain, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bolle Brands (France) SAS | Villeurbanne Rhone, France | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essilor International | CRETEIL Val-de-Marne, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essilor International, S.A. | LIGNY EN BARROIS Meuse, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essilor International, S.A. | DIJON Cote-d'Or, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jimmy Fairly | Paris, France | Contract manufacturer, Exporter to the US, Remanufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Julbo | LONGCHAUMOIS Jura, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sporoptic Pouilloux, SA | Paris, France | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.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.