Bodycap is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Bodycap - FDA 510(k) Cleared Devices
Recent clearances: e-Celsius Medical System
1
Total
1
Cleared
0
Denied
Bodycap has 1 FDA 510(k) cleared medical devices. Based in Herouville Saint Clair, FR.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bodycap Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Arazy Group Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bodycap
1 devices