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Grupo IX Kaan, S.A. de C.V.

US

Last updated May 27, 2026

What Grupo IX Kaan, S.A. de C.V. makes

Grupo IX Kaan, S.A. de C.V. manufactures reusable menstrual cups and discs made without latex, including variants in Crystal, Lilac, and Pink colors. These products are designed for menstrual hygiene and are intended for single-user, long-term use.

The company’s products fall under FDA Class II regulation and are 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 Grupo IX Kaan, S.A. de C.V. manufacture?

Grupo IX Kaan, S.A. de C.V. specializes in reusable menstrual cups and discs that do not contain latex. These products are designed for menstrual hygiene and are intended for single-user, long-term use. The company’s focus is on providing sustainable alternatives for menstrual care.

Where is Grupo IX Kaan, S.A. de C.V. based?

Grupo IX Kaan, S.A. de C.V. is based in the United States. The company’s location is relevant for understanding its regulatory environment and manufacturing operations.

How are the devices manufactured by Grupo IX Kaan, S.A. de C.V. classified under FDA regulations?

The devices produced by Grupo IX Kaan, S.A. de C.V., specifically their reusable menstrual cups and discs, are classified as Class II under FDA regulations. This classification typically indicates a moderate level of control is required to ensure their safety and effectiveness, as they are reusable and intended for internal use.

Are the devices manufactured by Grupo IX Kaan, S.A. de C.V. listed in any regulatory databases?

Yes, the devices manufactured by Grupo IX Kaan, S.A. de C.V. are included in the FDA’s Unique Device Identifier (UDI) database. This listing helps ensure traceability and transparency in the regulatory system, allowing for easier tracking of device history and compliance.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
+525555327858
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
951641030

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
Angelcup - Crystal Small Size
FDA UDI
Class IIActive
Angelcup - Crystal Large size
FDA UDI
Class IIActive
Angelcup - Lilac Small Size
FDA UDI
Class IIActive
Angelcup - Pink Large size
FDA UDI
Class IIActive
Angelcup - Pink Small Size
FDA UDI
Class IIActive
Angelcup - Lilac Large size
FDA UDI
Class IIActive

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