Medical Device Manufacturer · FR , Prunay Le Gillon

Luneau Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Luneau Sas has 2 FDA 510(k) cleared medical devices. Based in Prunay Le Gillon, FR.

Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Ophthalmic.

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

Luneau Sas is one of 151 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Luneau Sas

2 devices

1-2 of 2