Indiba USA, Inc. is one of 18404 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Indiba USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Indiba Diathermia Radiofrequency Device - Activ
1
Total
1
Cleared
0
Denied
Indiba USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Indiba USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Indiba S.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Indiba USA, Inc.
1 devices