# Neumodx Molecular, Inc.

- Location (FDA's records): Ann Arbor, MI
- FDA decisions: 2 (2018–2023): 2 510(k) clearances
- Product codes: QEP (1), NJR (1)
- Predicates its devices cite: 2 (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
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)
- Handylab, Inc.: 1 (https://510kreport.com/company/handylab)

## Recent decisions
- K230267: NeuMoDx CT/NG Assay 2.0 (Dec 22, 2023)
- K173725: NeuMoDx GBS Assay (Jun 26, 2018)

Source page: https://510kreport.com/company/neumodx-molecular