# Philips Hearing Instruments Co.

- Location (FDA's records): Mahwah, NJ
- FDA decisions: 20 (1991–1997): 20 510(k) clearances
- Product codes: ESD (20)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Insound Medical, Inc.: 2 (https://510kreport.com/company/insound-medical)
- Resound Corp.: 1 (https://510kreport.com/company/resound)

## Its most-cited devices
- K921725: Philip XP Series, in-the Canal Hearing Aid (1992), cited by 3

## Recent decisions
- K972818: D72 Digital (Oct 17, 1997)
- K971804: Philips S1694, S1695 (Jun 6, 1997)
- K965088: M11 Series: M11, M11M (Jan 24, 1997)
- K961770: Philips 71 Series (Aug 2, 1996)
- K952658: Hearing Aid (Jul 28, 1995)
- K944404: MO4 Series (Dec 27, 1994)
- K943670: MO6 Series (Aug 18, 1994)
- K943395: Philips M38 Series (Aug 9, 1994)

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