Stepone Fertility Ltd (T/A Béa Fertility)
United KingdomFDA applicant, unverified
- Devices
- 1
What Stepone Fertility Ltd (T/A Béa Fertility) makes
Stepone Fertility Ltd manufactures the Béa Applicator, a device designed for intrauterine insemination procedures to assist with sperm placement during fertility treatments.
The Béa Applicator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Béa Applicator (BAP-GB-01) Ref K242031
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stepone Fertility Ltd (T/A Béa Fertility) have in the registry?
The registry currently lists 1 device for Stepone Fertility Ltd (T/A Béa Fertility). Devices recorded under merged duplicate company entries are counted once.
Which registries list Stepone Fertility Ltd (T/A Béa Fertility)'s devices?
Among its 1 most recently registered device, Stepone Fertility Ltd (T/A Béa Fertility) has devices listed in FDA 510(k) (1 device).
What risk classes do Stepone Fertility Ltd (T/A Béa Fertility)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stepone Fertility Ltd (T/A Béa Fertility)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stepone Fertility Ltd (T/A Béa Fertility) in the registry?
The most recently registered devices listed for Stepone Fertility Ltd (T/A Béa Fertility) include Béa Applicator (BAP-GB-01).