Termosalud S.L. is one of 56 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: Zionic Pro Max (EMS), Zionic Pro Max (Radiofrequency)
2
Total
2
Cleared
0
Denied
Termosalud S.L. has 2 FDA 510(k) cleared medical devices. Based in Gijon, ES.
Latest FDA clearance: Mar 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 and Associates Regulatory Consulting and Hoy & Associates Regulatory Consulting, LLC.
FDA 510(k) Regulatory Record - Termosalud S.L.
2 devices