Abanza Tecnomed S.L is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Abanza Tecnomed S.L - FDA 510(k) Cleared Devices
Recent clearances: QuadLock™ Fixation System, WasherCap™ Fixation System, WasherCap™ Mini Fixation System (Model 45)
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.
FDA 510(k) Regulatory Record - Abanza Tecnomed S.L
4 devices