# Hearing Tech, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 11 (1985–1994): 11 510(k) clearances
- Product codes: ESD (10), MCW (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
- K941587: Hearing Tech (Jun 24, 1994)
- K924712: Rotablator Rotational Angioplasty System (Dec 8, 1992)
- K905680: 543 Series Bte (Mar 8, 1991)
- K903295: Escort Itc (Sep 5, 1990)
- K903023: Heritage Iii (HTC) Itc Type Hearing Aid (Jul 27, 1990)
- K870723: Heartech HFX, Hearing Aid (Mar 20, 1987)
- K870350: Escort EC Custom in-the-Ear Hearing Aid (Mar 11, 1987)
- K854315: Heartech Model in Tech (Jan 21, 1986)

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