Archeon is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Archeon - FDA 510(k) Cleared Devices
Recent clearances: EOlife®
1
Total
1
Cleared
0
Denied
Archeon has 1 FDA 510(k) cleared medical devices. Based in Besan?on, FR.
Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Archeon Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gloster Biomedical International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Archeon
1 devices