Indiba S. A. U. - FDA 510(k) Cleared 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.
3 devices