Fluoptics Sas (A Getinge Group Company) is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Fluoptics Sas (A Getinge Group Company) - FDA 510(k) Cleared Devices
Recent clearances: FLUOBEAM LX Imaging System (FBLX), FLUOBEAM® LX Imaging System (FB-LX)
2
Total
2
Cleared
0
Denied
Fluoptics Sas (A Getinge Group Company) has 2 FDA 510(k) cleared medical devices. Based in Grenoble, FR.
Latest FDA clearance: Apr 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fluoptics Sas (A Getinge Group Company) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Getinge Group as regulatory consultant.
FDA 510(k) Regulatory Record - Fluoptics Sas (A Getinge Group Company)
2 devices