# Gn Resound A/S

- Location (FDA's records): Ballerup, DK
- FDA decisions: 3 (2008–2015): 3 510(k) clearances
- Product codes: KLW (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 12 (2 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
- Spectral Visualization & Development, Inc.: 1 (https://510kreport.com/company/spectral-visualization-development)
- Siemens Hearing Instruments, Inc.: 1 (https://510kreport.com/company/siemens-hearing-instruments)

## Firms that cite its devices most
- Oticon A/S: 1 (https://510kreport.com/company/oticon-a-s)
- GN Hearing A/S: 1 (https://510kreport.com/company/gn-hearing-a-s)
- Unitron Hearing: 1 (https://510kreport.com/company/unitron-hearing)
- Starkey Laboratories, Inc.: 1 (https://510kreport.com/company/starkey-laboratories)
- Amplisound Hearing Products & Services: 1 (https://510kreport.com/company/amplisound-hearing-products-services)
- Magnatone Hearing Aid Corp. Dba Persona Medical: 1 (https://510kreport.com/company/magnatone-hearing-aid-dba-persona-medical)
- Kw Ear Lab, Inc.: 1 (https://510kreport.com/company/kw-ear-lab)
- Soundcure, Inc.: 1 (https://510kreport.com/company/soundcure)

## Its most-cited devices
- K110932: Tinnitus Sound Generator Module (2011), cited by 7
- K073636: Tinnitus Sound Generator Module (2008), cited by 4
- K150171: Tinnitus Sound Generator Module (2015), cited by 1

## Recent decisions
- K150171: Tinnitus Sound Generator Module (May 14, 2015)
- K110932: Tinnitus Sound Generator Module (May 3, 2011)
- K073636: Tinnitus Sound Generator Module (Mar 13, 2008)

Source page: https://510kreport.com/company/gn-resound-a-s