Abanza Tecnomed S.L - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Abanza Tecnomed S.L has 4 FDA 510(k) cleared medical devices. Based in Mutilva, ES.
Latest FDA clearance: Jan 2026. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Abanza Tecnomed S.L Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Precision Life Science Partners and Presicion Life Science Partners.
4 devices