# Miracle-Ear/Dahlberg, Inc.

- Location (FDA's records): Golden Valley, MN
- FDA decisions: 23 (1985–1994): 23 510(k) clearances
- Product codes: ESD (22), EWO (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
- K942894: Miracle-Ear Model PGC (Aug 17, 1994)
- K942895: Miracle Ear Model PGM (Aug 17, 1994)
- K942893: Miracle-Ear Model PGF + Remote (Aug 17, 1994)
- K941859: Miracle-Ear Ear Impression Material (Jul 25, 1994)
- K862101: Model UM in-the-Canal Hearing Aid (Jun 23, 1986)
- K862102: Model KM in-the-Canal Hearing Aid (Jun 23, 1986)
- K862099: Dahlberg Model EE Behind-the-Ear Hearing Aid (Jun 23, 1986)
- K862104: Model UC Spectrum in-the-Canal Hearing Aid (Jun 23, 1986)

Source page: https://510kreport.com/company/miracle-ear-dahlberg