Luneau SA
FranceFDA applicant, unverified
- Devices
- 5
What Luneau SA makes
Luneau SA makes medical devices such as tonometer separation prisms, 3 mirror lenses, and anesthesiometers. These products are used in ophthalmology and other medical fields.
The company's portfolio is regulated and listed in the FDA 510(k) registry, with devices classified as Class I and Class II. Luneau SA is based in the US.
Catalogue
VX120 Ophthalmic Diagnostic Device Ref K143086
Regimes: 510(k) Registry: 510(k)VX130 Ophthalmic Diagnostic Device Ref K162067
Regimes: 510(k) Registry: 510(k)Luneau Sterile Tonometer Separation Prisms Ref K023838
Regimes: 510(k) Registry: 510(k)Luneau 3 Mirror Lens Ref K022413
Regimes: 510(k) Registry: 510(k)Anesthesiometer Ref K851557
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luneau SA have in the registry?
The registry currently lists 5 devices for Luneau SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luneau SA's devices?
Among its 5 most recently registered devices, Luneau SA has devices listed in FDA 510(k) (5 devices).
What risk classes do Luneau SA's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Luneau SA's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luneau SA in the registry?
The most recently registered devices listed for Luneau SA include VX120 Ophthalmic Diagnostic Device, VX130 Ophthalmic Diagnostic Device, LUNEAU STERILE TONOMETER SEPARATION PRISMS and LUNEAU 3 MIRROR LENS.