# Ekeroth Quality AB

- Location (FDA's records): Stockholm, SE
- FDA decisions: 1 (1999–1999): 1 510(k) clearance
- Product codes: LNH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Choy Medical Technologies, Inc.: 1 (https://510kreport.com/company/choy-medical-technologies)

## Its most-cited devices
- K992120: Dynawell or Dynawell (1999), cited by 1

## Recent decisions
- K992120: Dynawell or Dynawell (Aug 13, 1999)

Source page: https://510kreport.com/company/ekeroth-quality