Indiba S. A. U. is one of 56 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Indiba S. A. U. - FDA 510(k) Cleared Devices
Recent clearances: Indiba Diathermia Radiofrequency Deep Care Device (Deep care IDC0409/EVONY ), Reverso Pro System, INDIBA COMPACT devices
3
Total
3
Cleared
0
Denied
Indiba S. A. U. has 3 FDA 510(k) cleared medical devices. Based in Sant Quirze Del Vall?s (Barcelona), ES.
Latest FDA clearance: Jan 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Indiba S. A. U. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by A. Stein Regulatory Affairs Consulting Company , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Indiba S. A. U.
3 devices