Corify Care S.L - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Corify Care S.L has 1 FDA 510(k) cleared medical devices. Based in Madrid, ES.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Corify Care S.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Freyr, Inc. as regulatory consultant.
1 devices