# Luneau Ophtalmologie SA

- Location (FDA's records): Chartres Cedex, FR
- FDA decisions: 3 (1991–1992): 3 510(k) clearances
- Product codes: HOS (1), HMF (1), HLQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K922253: Keratoref L60 (Jun 19, 1992)
- K921214: Ophthalmic Projector (Jun 11, 1992)
- K913961: Ophthalmic Stand (Dec 4, 1991)

Source page: https://510kreport.com/company/luneau-ophtalmologie