STEPONE FERTILITY LTD
US Last updated 30 May 2026 Part of Stepone Fertility Ltd
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- Devices
- 2
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
Béa Fertility BTK-US-01 Ref BTK-US-01
Béa Fertility BAP-GB-01 Ref BAP-GB-01
FDA establishments
- Stepone Fertility Ltd London Westminster · GB FEI 3038597712
What STEPONE FERTILITY LTD makes
The company manufactures single-use cervical caps designed for contraception, including the Béa Fertility device. These products are intended for barrier contraception during intercourse and are positioned as reusable alternatives in a single-use format.
The portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Information
- Country
- US
- DUNS number
- 225808762