Leloi AB
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Leloi AB is a medical device manufacturer, with 37 devices listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.
- Devices
- 37
Registry facts
- Registries
- FDA GUDID 37
- Device classes
- FDA Class II 37
- Identifiers
- DUNS 508701849
What Leloi AB makes
Leloi AB manufactures basic male condoms made from Hevea-latex, including lubricated and non-lubricated varieties, as well as penile rings. The company also produces reusable menstrual cups and discs in non-latex materials, designed for pelvic floor strength training and menstrual hygiene. Additional products include a perineometer, a device used to measure pelvic floor muscle strength.
These products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 37 devicesCompany details
- DUNS number
- 508701849
Frequently asked questions
How many devices does Leloi AB have in the registry?
The registry currently lists 37 devices for Leloi AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leloi AB's devices?
Among its 37 most recently registered devices, Leloi AB has devices listed in FDA GUDID (37 devices).
What risk classes do Leloi AB's devices fall under?
Among its 37 most recently registered devices, the classes recorded for Leloi AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leloi AB in the registry?
The most recently registered devices listed for Leloi AB include Lelo Hex Lubricated Natural Rubber Latex Condom collection 3 pack, Lelo Hex Lubricated Natural Rubber Latex Condom collection 12 pack, Lelo Hex Lubricated Natural Rubber Latex Condom 36’s 36s and Intimina Kegel Smart 2 Plus Soft Pink.