# Dyn'R Sas

- Location (FDA's records): Aix En Provence, FR
- FDA decisions: 2 (2010–2012): 2 510(k) clearances
- Names in FDA's records: Dyn'R Sas (1); Dyn'R (1)
- Product codes: IYE (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- Varian Medical Systems, Inc.: 1 (https://510kreport.com/company/varian-medical-systems)
- Aktina Medical Physics Corp.: 1 (https://510kreport.com/company/aktina-medical-physics)

## Its most-cited devices
- K092479: SDX-Spirodynr'x Radiotherapy Breathing Control (2010), cited by 1

## Recent decisions
- K121845: SDX System (Oct 19, 2012)
- K092479: SDX-Spirodynr'x Radiotherapy Breathing Control (Jan 11, 2010)

Source page: https://510kreport.com/company/dyn-r