Clarteis is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Clarteis - FDA 510(k) Cleared Devices
Recent clearances: Exciplex
2
Total
2
Cleared
0
Denied
Clarteis has 2 FDA 510(k) cleared medical devices. Based in Valbonne, FR.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Clarteis Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Clarteis
2 devices