# Gn Danavox, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 10 (1986–1997): 10 510(k) clearances
- Product codes: ESD (9), ETW (1)
- Predicates its devices cite: 2 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K905692: 143 Series Bte (1991), cited by 2

## Recent decisions
- K971032: Danavox Models 163/162 Bte (Jun 17, 1997)
- K971031: Audallion Iii Hearing System (Jun 17, 1997)
- K942331: Danavox Model Cic (Nov 15, 1994)
- K924185: DFS Genius Bte (Nov 3, 1992)
- K905692: 143 Series Bte (Jan 28, 1991)
- K905679: 133 Series Bte (Jan 28, 1991)
- K896996: Cas (Computerized Analyzer System) (Aug 9, 1990)
- K896995: Discretion, in the Canal Hearing Instrument (Apr 30, 1990)

Source page: https://510kreport.com/company/gn-danavox