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Maevespads LLC

US

Last updated May 31, 2026

What Maevespads LLC makes

Maevespads LLC manufactures unscented menstrual pads designed for menstrual hygiene. The product line includes disposable pads marketed under the Maeves brand, focusing on comfort and absorbency for daily use.

The company’s products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. Maevespads LLC operates from 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 Maevespads LLC manufacture?

Maevespads LLC specializes in menstrual hygiene products, specifically unscented disposable menstrual pads under the Maeves brand. These pads are designed for daily use, focusing on comfort and absorbency. Since menstrual pads are classified as Class I devices by the FDA, they are considered low-risk and generally do not require stringent pre-market approvals beyond registration and listing.

Where is Maevespads LLC based?

Maevespads LLC is headquartered in the United States. The company’s location is relevant for regulatory purposes, as it determines which national authorities oversee compliance and reporting requirements for its devices.

Are Maevespads LLC’s devices listed in any regulatory registries?

Yes, Maevespads LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency in the supply chain and regulatory oversight. Listing in this database is mandatory for Class I devices in the U.S. to facilitate traceability.

How are Maevespads LLC’s menstrual pads classified by regulatory authorities?

Maevespads LLC’s menstrual pads are classified as FDA Class I medical devices. This classification is based on their intended use—disposable menstrual hygiene products—and their low-risk profile. Class I devices typically undergo general controls (like registration, labeling, and manufacturing practices) rather than specialized pre-market reviews, as they pose minimal risk to users.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
065944990

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Maeves Pads, Maeves MAEVES-245
FDA UDI
Class IActive
Maeves Pads, Maeves MAEVES-290
FDA UDI
Class IActive
Maeves Pads, Maeves MAEVES-360
FDA UDI
Class IActive

Related Companies

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