Medical Device Manufacturer · FR , Chartres Cedex

Luneau SA - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1985

Total

Cleared

Denied

Luneau SA has 3 FDA 510(k) cleared medical devices. Based in Chartres Cedex, FR.

Historical record: 3 cleared submissions from 1985 to 2003. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Luneau SA Filter by specialty or product code using the sidebar.

Luneau SA is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Luneau SA

3 devices

1-3 of 3