# Unisensor AG

- Location (FDA's records): Golden, CO
- FDA decisions: 2 (2001–2007): 2 510(k) clearances
- Product codes: FFX (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 4 (1 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
- Sierra Scientific Instruments, Inc.: 1 (https://510kreport.com/company/sierra-scientific-instruments)

## Firms that cite its devices most
- E-Cath Co., Ltd.: 2 (https://510kreport.com/company/e-cath)
- Diversatek Healthcare: 1 (https://510kreport.com/company/diversatek-healthcare)

## Its most-cited devices
- K062222: Unitip High Resolution Catheter (2007), cited by 2
- K003580: Unitip Gastrointestinal Pressure Sensor Catheter (2001), cited by 2

## Recent decisions
- K062222: Unitip High Resolution Catheter (Mar 15, 2007)
- K003580: Unitip Gastrointestinal Pressure Sensor Catheter (Jul 31, 2001)

Source page: https://510kreport.com/company/unisensor