# Rhythm Xience, Inc. (Rxi)

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 2 (2017–2017): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- St Jude Medical: 2 (https://510kreport.com/company/st-jude-medical)

## Firms that cite its devices most
- Acutus Medical, Inc.: 2 (https://510kreport.com/company/acutus-medical)

## Its most-cited devices
- K171081: Guider Catheter Introducer (2017), cited by 1
- K170373: Flextra Steerable Introducer (2017), cited by 1

## Recent decisions
- K171081: Guider Catheter Introducer (May 9, 2017)
- K170373: Flextra Steerable Introducer (Feb 27, 2017)

Source page: https://510kreport.com/company/rhythm-xience-rxi