# Neko Health AB

- Location (FDA's records): Danderyd, SE
- FDA decisions: 3 (2026–2026): 3 510(k) clearances
- Product codes: LHQ (1), MUD (1), QOK (1)
- Predicates its devices cite: 3 (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
- Thermidas Americas, Inc.: 1 (https://510kreport.com/company/thermidas-americas)
- Modulated Imaging, Inc.: 1 (https://510kreport.com/company/modulated-imaging)
- Continuse Biometrics, Ltd.: 1 (https://510kreport.com/company/continuse-biometrics)

## Recent decisions
- K254240: Echo-2 (Sep 22, 2026)
- K254129: Spectrum-2 (May 22, 2026)
- K253911: Derma-2 (May 20, 2026)

Source page: https://510kreport.com/company/neko-health