Bluesom is one of 151 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Bluesom - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bluesom has 1 FDA 510(k) cleared medical devices. Based in Orvault, FR.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bluesom Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bluesom
1 devices