CorDx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
CorDx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CorDx Tyfast COVID-19 Ag Rapid Test Rx, CorDx Tyfast COVID-19 Ag Rapid Test
2
Total
2
Cleared
0
Denied
CorDx, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by CorDx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - CorDx, Inc.
2 devices