# Lumos Diagnostics, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 2 (2023–2026): 2 510(k) clearances
- Product codes: QXA (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Cd Diagnostics, Inc.: 1 (https://510kreport.com/company/cd-diagnostics)

## Its most-cited devices
- K230917: FebriDx Bacterial / Non-bacterial Point of Care Assay (2023), cited by 1

## Recent decisions
- K260787: FebriDx Bacterial/Non-bacterial Assay (Mar 24, 2026)
- K230917: FebriDx Bacterial / Non-bacterial Point of Care Assay (Jun 30, 2023)

Source page: https://510kreport.com/company/lumos-diagnostics