# Indiba USA, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: PBX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cutera, Inc.: 1 (https://510kreport.com/company/cutera)
- Ellman International, Inc.: 1 (https://510kreport.com/company/ellman-international)

## Firms that cite its devices most
- Indiba S. A. U.: 2 (https://510kreport.com/company/indiba-s-a-u)
- Termosalud: 1 (https://510kreport.com/company/termosalud)
- Capenergy Medical S.L.: 1 (https://510kreport.com/company/capenergy-medical)
- Xod, Inc.: 1 (https://510kreport.com/company/xod)
- Wintecare SA: 1 (https://510kreport.com/company/wintecare)

## Its most-cited devices
- K161458: Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care (2016), cited by 6

## Recent decisions
- K161458: Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care (Oct 3, 2016)

Source page: https://510kreport.com/company/indiba-usa