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Kimberly Clark Costa Rica Ltda

US

Last updated May 30, 2026

Part of KIMBERLY-CLARK COSTA RICA, Ltda

What Kimberly Clark Costa Rica Ltda makes

Kimberly Clark Costa Rica Ltda manufactures unscented menstrual pads designed for personal hygiene. These products are marketed under the Kotex brand and are intended for disposable use during menstruation.

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 operates from Costa Rica, though its products are regulated under US medical device standards.

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 Kimberly Clark Costa Rica Ltda manufacture?

Kimberly Clark Costa Rica Ltda specializes in unscented menstrual pads, which are disposable hygiene products marketed under the Kotex brand. These devices are designed for personal use during menstruation and fall under the category of feminine hygiene products.

Where is Kimberly Clark Costa Rica Ltda based, and under which country’s regulations are its devices regulated?

The company is based in Costa Rica, but its products are regulated under US medical device standards. This means its devices comply with the requirements set by the US Food and Drug Administration (FDA), even though the manufacturer operates outside the US.

Which regulatory registries or databases list Kimberly Clark Costa Rica Ltda’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning a standardized identification number to each product, ensuring traceability and regulatory compliance.

How are Kimberly Clark Costa Rica Ltda’s devices classified by the FDA?

The company’s menstrual pads are classified as FDA Class I medical devices. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, such as disposable hygiene products, and generally require less stringent regulatory oversight.

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

Information

Country
US
Address
—
Website
kcc.com
LinkedIn
—
Facebook
—
Phone
+5068008002473
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
853201189

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Kotex Pad
FDA UDI
Class IActive
Kotex Pad
FDA UDI
Class IActive
Kotex Pad
FDA UDI
Class IActive
Kotex Pad
FDA UDI
Class IActive

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