Luneau Ophtalmologie SA
FranceFDA applicant, unverified
- Devices
- 3
What Luneau Ophtalmologie SA makes
Luneau Ophtalmologie SA manufactures ophthalmic devices including the KERATOREF L60, an ophthalmic projector, and an ophthalmic stand.
The company's devices are classified as Class I and are listed in the FDA 510(k) registry. Luneau Ophtalmologie SA is based in the US.
Catalogue
Keratoref L60 Ref K922253
Regimes: 510(k) Registry: 510(k)Ophthalmic Projector Ref K921214
Regimes: 510(k) Registry: 510(k)Ophthalmic Stand Ref K913961
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luneau Ophtalmologie SA have in the registry?
The registry currently lists 3 devices for Luneau Ophtalmologie SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luneau Ophtalmologie SA's devices?
Among its 3 most recently registered devices, Luneau Ophtalmologie SA has devices listed in FDA 510(k) (3 devices).
What risk classes do Luneau Ophtalmologie SA's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Luneau Ophtalmologie SA's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Luneau Ophtalmologie SA in the registry?
The most recently registered devices listed for Luneau Ophtalmologie SA include KERATOREF L60, OPHTHALMIC PROJECTOR and OPHTHALMIC STAND.