Pherdal Fertility Science, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3020796587
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
PherDal® At-Home Insemination Kit Ref K231645
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020796587
- Address
- 2238 Pine Bluff Dr, Dixon, IL, 61021
Frequently asked questions
How many devices does Pherdal Fertility Science, Inc. have in the registry?
The registry currently lists 2 devices for Pherdal Fertility Science, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pherdal Fertility Science, Inc.'s devices?
Among its 2 most recently registered devices, Pherdal Fertility Science, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pherdal Fertility Science, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pherdal Fertility Science, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pherdal Fertility Science, Inc. in the registry?
The most recently registered devices listed for Pherdal Fertility Science, Inc. include PherDal At-Home Insemination Kit and PherDal® At-Home Insemination Kit.