Ancestry Genomics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ancestry Genomics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AncestryDNA Factor V Leiden Genetic Health Risk Test, AncestryDNA Saliva Collection Kit
2
Total
2
Cleared
0
Denied
Ancestry Genomics, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Ancestry Genomics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ancestry Genomics, Inc.
2 devices