Immunexpress, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immunexpress, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SeptiCyte RAPID, SeptiCyte RAPID
3
Total
3
Cleared
0
Denied
Immunexpress, Inc. has 3 FDA 510(k) cleared medical devices. Based in Seattle, US.
Last cleared in 2023. Active since 2017. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Immunexpress, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Immunexpress, Inc.
3 devices