Neumodx Molecular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neumodx Molecular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeuMoDx CT/NG Assay 2.0, NeuMoDx GBS Assay
2
Total
2
Cleared
0
Denied
Neumodx Molecular, Inc. has 2 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.
Last cleared in 2023. Active since 2018. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Neumodx Molecular, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medical Device Regulatory Solutions, LLC and Qiagen.
FDA 510(k) Regulatory Record - Neumodx Molecular, Inc.
2 devices