Ancestry Genomics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ancestry Genomics, Inc. makes
Ancestry Genomics, Inc. manufactures genetic testing kits, including the AncestryDNA Saliva Collection Kit for ancestry analysis and the AncestryDNA Factor V Leiden Genetic Health Risk Test for hereditary risk assessment.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
AncestryDNA Saliva Collection Kit Ref K192947
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ancestry Genomics, Inc. have in the registry?
The registry currently lists 2 devices for Ancestry Genomics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ancestry Genomics, Inc.'s devices?
Among its 2 most recently registered devices, Ancestry Genomics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ancestry Genomics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ancestry Genomics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ancestry Genomics, Inc. in the registry?
The most recently registered devices listed for Ancestry Genomics, Inc. include AncestryDNA Saliva Collection Kit and AncestryDNA Factor V Leiden Genetic Health Risk Test.