# Neurotherapies Reset GmbH

- Location (FDA's records): Juelich, DE
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: KLW (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
- K151558: Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System (Jan 20, 2016)

Source page: https://510kreport.com/company/neurotherapies-reset