Kama Sutra
Country not established
- Devices
- 1
What Kama Sutra makes
The company produces personal lubricants designed for sexual use, including water-based formulations intended to enhance comfort and reduce friction during intimate activities.
The portfolio is regulated as Class II medical devices in the US and is listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 053877858
- [email protected]
- Phone
- 8007787921
Frequently asked questions
How many devices does Kama Sutra have in the registry?
The registry currently lists 1 device for Kama Sutra. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kama Sutra's devices?
Among its 1 most recently registered device, Kama Sutra has devices listed in FDA GUDID (1 device).
What risk classes do Kama Sutra's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kama Sutra's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kama Sutra in the registry?
The most recently registered devices listed for Kama Sutra include Kama Sutra Love Liquid Personal Lubricant 10210.