# Phonak, Inc.

- Location (FDA's records): Naperville, IL
- FDA decisions: 39 (1990–2013): 39 510(k) clearances
- Names in FDA's records: Phonak, Inc. (37); Phonak, LLC (2)
- Product codes: ESD (37), EPF (1), KLW (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (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
- Insound Medical, Inc.: 2 (https://510kreport.com/company/insound-medical)
- Gn Resound A/S: 1 (https://510kreport.com/company/gn-resound-a-s)
- Widex USA: 1 (https://510kreport.com/company/widex-usa)
- Siemens Hearing Instruments, Inc.: 1 (https://510kreport.com/company/siemens-hearing-instruments)

## Firms that cite its devices most
- Oticon A/S: 1 (https://510kreport.com/company/oticon-a-s)
- Sonova AG: 1 (https://510kreport.com/company/sonova)

## Its most-cited devices
- K130790: LYRIC2 (2013), cited by 1
- K123450: Phonak Tinnitus Balance (2013), cited by 1

## Recent decisions
- K130790: LYRIC2 (Jun 27, 2013)
- K123450: Phonak Tinnitus Balance (Feb 11, 2013)
- K972106: Phonak Novo Forte E3 (Aug 15, 1997)
- K972105: Phonak Epica (Aug 1, 1997)
- K972097: Phonak Microzoom P 2 (Jul 30, 1997)
- K964035: Phonak Microlink, Personal FM Receiver (Dec 4, 1996)
- K961653: Phonak Sona P2 (May 29, 1996)
- K961622: Phonak PICONET2 P2 AZ (May 17, 1996)

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