Genosis, Inc.
Also registered as Genosis, Ltd.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Fertell Male Fertility Test Ref K041039
Regimes: 510(k) Registry: 510(k)Fertell Female Fertility Test Ref K032002
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genosis, Inc. have in the registry?
The registry currently lists 2 devices for Genosis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genosis, Inc.'s devices?
Among its 2 most recently registered devices, Genosis, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Genosis, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Genosis, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genosis, Inc. in the registry?
The most recently registered devices listed for Genosis, Inc. include FERTELL MALE FERTILITY TEST and FERTELL FEMALE FERTILITY TEST.