Ceres Fertility, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ceres Fertility, Inc. makes
Ceres Fertility, Inc. manufactures sperm wash media, including the PROMOTOR FINAL RINSE SPERM WASH MEDIUM and PROMOTOR, which are used in fertility treatments.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Promotor Final Rinse Sperm Wash Medium Ref K024290
Regimes: 510(k) Registry: 510(k)Promotor Ref K023106
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ceres Fertility, Inc. have in the registry?
The registry currently lists 2 devices for Ceres Fertility, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ceres Fertility, Inc.'s devices?
Among its 2 most recently registered devices, Ceres Fertility, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ceres Fertility, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ceres Fertility, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ceres Fertility, Inc. in the registry?
The most recently registered devices listed for Ceres Fertility, Inc. include PROMOTOR FINAL RINSE SPERM WASH MEDIUM and PROMOTOR.