Eurobio is one of 254 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Eurobio - FDA 510(k) Cleared Devices
Recent clearances: Cornea Cold
1
Total
1
Cleared
0
Denied
Eurobio has 1 FDA 510(k) cleared medical devices. Based in Les Ulis, FR.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eurobio Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by International Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Eurobio
1 devices