# Lumendo AG

- Location (FDA's records): Renens, CH
- FDA decisions: 2 (2023–2023): 2 510(k) clearances
- Product codes: KIF (1), QNF (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
- Sonendo, Inc.: 1 (https://510kreport.com/company/sonendo)
- Ultradent Products, Inc.: 1 (https://510kreport.com/company/ultradent-products)
- Foshan Coxo Medical Instrument Co., Ltd.: 1 (https://510kreport.com/company/foshan-coxo-medical-instrument)

## Recent decisions
- K232076: Fibercure (Nov 2, 2023)
- K231387: Endofill (Jul 10, 2023)

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