# Widex Hearing Aid Co., Inc.

- Location (FDA's records): Long Island City, NY
- FDA decisions: 52 (1976–2008): 52 510(k) clearances
- Product codes: ESD (51), KLW (1)
- Predicates its devices cite: 3 (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
- Neuromonics Pty, Ltd.: 1 (https://510kreport.com/company/neuromonics)
- Siemens Hearing Instruments, Inc.: 1 (https://510kreport.com/company/siemens-hearing-instruments)
- Petroff Audio Technologies: 1 (https://510kreport.com/company/petroff-audio-technologies)

## Firms that cite its devices most
- Widex USA: 1 (https://510kreport.com/company/widex-usa)

## Its most-cited devices
- K080955: Zen Program (Mind 440 Hearing Aid) (2008), cited by 1

## Recent decisions
- K080955: Zen Program (Mind 440 Hearing Aid) (Jun 27, 2008)
- K971535: Widex Senso Digital (Mini Canal) (Jun 6, 1997)
- K970904: Widex Senso Digital (Cic) (Mar 26, 1997)
- K965254: Widex Model Senso Digital (C9) (Mar 12, 1997)
- K965218: Senso Digital (C18) (Jan 24, 1997)
- K955879: Widex Model Senso Digital (C16) (Feb 27, 1996)
- K955878: Widex Model Senso Digital (C8) (Feb 12, 1996)
- K954526: Widex Senso Digital (PX) (Oct 18, 1995)

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