Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Femmepharma Consumer Healthcare, LLC

US

Last updated May 31, 2026

What Femmepharma Consumer Healthcare, LLC makes

Femmepharma Consumer Healthcare, LLC produces personal lubricants designed for intimate use, including water-based and silicone-based formulations. Their portfolio includes products like Mia Vita and Satisfaite, which are intended to enhance comfort and reduce friction during sexual activity.

These products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Femmepharma Consumer Healthcare, LLC manufacture?

Femmepharma Consumer Healthcare, LLC specializes in personal lubricants for intimate use, including water-based and silicone-based formulations. These products are designed to enhance comfort and reduce friction during sexual activity, addressing a specific consumer healthcare need.

Where is Femmepharma Consumer Healthcare, LLC based?

The company is headquartered in the United States, operating within the domestic market for its medical device products.

Which regulatory databases list Femmepharma Consumer Healthcare, LLC’s devices?

The company’s devices are included in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries help track and identify medical devices that have undergone the necessary regulatory processes.

How are Femmepharma Consumer Healthcare, LLC’s devices classified under FDA regulations?

Femmepharma’s products, such as sexual lubricants like Mia Vita and Satisfaite, are classified as Class II medical devices. This classification is based on their intended use and risk profile, requiring compliance with specific FDA controls to ensure safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
610-995-0801
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
116647151

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Mia Vita 01
FDA UDI
Class IIActive
Satisfaite K190752
FDA 510(k)FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.