# Unitron Hearing

- Location (FDA's records): Plymouth, MN
- FDA decisions: 1 (2013–2013): 1 510(k) clearance
- Product codes: KLW (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Gn Resound A/S: 1 (https://510kreport.com/company/gn-resound-a-s)

## Firms that cite its devices most
- Sanuthera, Inc.: 1 (https://510kreport.com/company/sanuthera)

## Its most-cited devices
- K130494: Unitron Tinnitus Masker Feature (2013), cited by 1

## Recent decisions
- K130494: Unitron Tinnitus Masker Feature (May 7, 2013)

Source page: https://510kreport.com/company/unitron-hearing