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The Kama Sutra Company

Country not established FDA establishment FEI 1000375074

Devices
1
Registrations
FDA
FDA recalls
0

What The Kama Sutra Company makes

The Kama Sutra Company makes Love Liquid Personal Lubricant, a personal lubricant product.

This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Company details

FDA FEI number
1000375074
Address
5260 Kazuko Ct, Moorpark, CA, 93021

Frequently asked questions

How many devices does THE KAMA SUTRA COMPANY have in the registry?

The registry currently lists 1 device for THE KAMA SUTRA COMPANY. Devices recorded under merged duplicate company entries are counted once.

Which registries list THE KAMA SUTRA COMPANY's devices?

Among its 1 most recently registered device, THE KAMA SUTRA COMPANY has devices listed in FDA 510(k) (1 device).

What risk classes do THE KAMA SUTRA COMPANY's devices fall under?

Among its 1 most recently registered device, the classes recorded for THE KAMA SUTRA COMPANY's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from THE KAMA SUTRA COMPANY in the registry?

The most recently registered devices listed for THE KAMA SUTRA COMPANY include Love Liquid Personal Lubricant.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.