# Turtle Beach Corporation

- Location (FDA's records): San Diego, CA
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: KLW (1)
- Predicates its devices cite: 2 (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
- Gn Resound A/S: 1 (https://510kreport.com/company/gn-resound-a-s)
- Soundcure, Inc.: 1 (https://510kreport.com/company/soundcure)

## Recent decisions
- K161331: HyperSound Tinnitus Module (Aug 23, 2016)

Source page: https://510kreport.com/company/turtle-beach