# The Siesta Group North America

- Location (FDA's records): Dedham, MA
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: MNR (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Widemed, Ltd.: 1 (https://510kreport.com/company/widemed)

## Firms that cite its devices most
- Younes Sleep Technologies: 1 (https://510kreport.com/company/younes-sleep-technologies)
- Respironics, Inc.: 1 (https://510kreport.com/company/respironics)

## Its most-cited devices
- K083620: Somnolyzer 24X7 (2009), cited by 2

## Recent decisions
- K083620: Somnolyzer 24X7 (Mar 6, 2009)

Source page: https://510kreport.com/company/siesta-group-north-america