# Danavox, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 26 (1977–1994): 26 510(k) clearances
- Product codes: ESD (25), KLW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K940608: 155 PP Agc-I (May 4, 1994)
- K851069: Body Type Hearing Aid 107S (Jun 5, 1985)
- K843791: Behind-the-Ear 123 VTH (Nov 9, 1984)
- K833486: IN-the-Ear Hearing Aid Model (Jun 22, 1984)
- K832326: Behind-the-Ear #123 Agci (Sep 29, 1983)
- K832751: Behind-the-Ear Series 125 (Sep 29, 1983)
- K823073: 101M in-the-Ear (Jan 7, 1983)
- K823531: Behind-the-Ear Hearing Aid #8003 (Dec 15, 1982)

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