# Finetone Hearing Instruments

- Location (FDA's records): Scarborough, ME
- FDA decisions: 5 (1983–1998): 5 510(k) clearances
- Product codes: ESD (4), LRB (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
- K974219: Faceplate Assembly (Feb 20, 1998)
- K955692: Finetone FSC, (Feb 2, 1996)
- K945780: Finetone Disceet Canal (Dec 21, 1994)
- K940164: Super-Sil (Jun 29, 1994)
- K830960: Custom in-the-Ear Hearing Aid (Jun 30, 1983)

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