Fluoptics Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Fluoptics Sas - FDA 510(k) Cleared Devices
Recent clearances: FLUOBEAM® LX Red
1
Total
1
Cleared
0
Denied
Fluoptics Sas has 1 FDA 510(k) cleared medical devices. Based in Grenoble, FR.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fluoptics Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Getinge as regulatory consultant.
FDA 510(k) Regulatory Record - Fluoptics Sas
1 devices