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Athena Medical Products Inc.

US

Last updated May 30, 2026

What Athena Medical Products Inc. makes

Athena Medical Products Inc. manufactures general-body orifice lubricants, including the EZ product line, designed for use in medical procedures requiring lubrication of body orifices.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Athena Medical Products Inc. manufacture?

Athena Medical Products Inc. specializes in general-body orifice lubricants. These products are designed to provide lubrication during medical procedures involving body orifices, such as examinations or minor interventions. The company’s focus is on ensuring smooth application in clinical settings where such lubrication is required.

Where is Athena Medical Products Inc. based?

Athena Medical Products Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device standards.

Which regulatory registries list Athena Medical Products Inc.’s devices?

Athena Medical Products Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare supply chain.

How are Athena Medical Products Inc.’s devices classified by the FDA?

Athena Medical Products Inc.’s devices fall under FDA’s Class I classification. This classification is assigned to low-risk medical devices that pose minimal potential harm to patients, often requiring less stringent regulatory oversight than higher-risk categories.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
1-800-523-8337
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
079346397

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Ez 000304
FDA UDI
Class IActive
Ez 000302
FDA UDI
Class IActive

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