# Sonowand AS

- Location (FDA's records): Ne, MN
- FDA decisions: 2 (2009–2012): 2 510(k) clearances
- Product codes: HAW (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (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
- Brainlab AG: 1 (https://510kreport.com/company/brainlab)
- General Electric Co.: 1 (https://510kreport.com/company/general-electric)
- Siemens Medical Solutions USA, Inc., Ultrasound DI: 1 (https://510kreport.com/company/siemens-medical-solutions-usa-ultrasound-di)

## Firms that cite its devices most
- Intravent Medical Partners, LP: 2 (https://510kreport.com/company/intravent-medical-partners)

## Its most-cited devices
- K083597: Sonowand Invite (2009), cited by 2
- K112469: General Prupose Localizers and Adapters-New Accessories for Sonowand System (2012), cited by 1

## Recent decisions
- K112469: General Prupose Localizers and Adapters-New Accessories for Sonowand System (Mar 23, 2012)
- K083597: Sonowand Invite (Sep 25, 2009)

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