Termosalud S.L. is one of 84 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Termosalud S.L. - FDA 510(k) Cleared Devices
Recent clearances: Chromix, Zionic Pro Max (EMS), Zionic Pro Max (Radiofrequency)
3
Total
3
Cleared
0
Denied
Termosalud S.L. has 3 FDA 510(k) cleared medical devices. Based in Gijon, ES.
Latest FDA clearance: Jul 2026. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Termosalud S.L. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hoy & Associates Regulatory Consulting, LLC and Hoy and Associates Regulatory Consulting.
FDA 510(k) Regulatory Record - Termosalud S.L.
3 devices