# Hearing Innovations, Inc.

- Location (FDA's records): Washington, D.C., DC
- FDA decisions: 3 (1995–2002): 3 510(k) clearances
- Product codes: ESD (1), KLW (1), LXB (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 2 (1 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
- 3M Company: 2 (https://510kreport.com/company/3m)
- Starkey Laboratories, Inc.: 2 (https://510kreport.com/company/starkey-laboratories)
- Resound Corp.: 1 (https://510kreport.com/company/resound)
- Siemens Hearing Instruments, Inc.: 1 (https://510kreport.com/company/siemens-hearing-instruments)
- Adm Tronics Unltd, Inc.: 1 (https://510kreport.com/company/adm-tronics-unltd)

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

## Its most-cited devices
- K013253: Hisonic-TRD Tinnitus Relief Device (2002), cited by 1
- K951678: HI Sonic 2000 Digital Hearing Instrument (1995), cited by 1

## Recent decisions
- K013253: Hisonic-TRD Tinnitus Relief Device (Apr 5, 2002)
- K963745: Model WMR Bte Hearing Instrument (Model WMR) (Nov 26, 1996)
- K951678: HI Sonic 2000 Digital Hearing Instrument (Jun 7, 1995)

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