# Goldenear Company, Inc.

- Location (FDA's records): Santa Clarita, CA
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: KLW (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Kw Ear Lab, Inc.: 1 (https://510kreport.com/company/kw-ear-lab)

## Recent decisions
- K221168: Tinnitogram Signal Generator (Feb 1, 2023)

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