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Naturalena Brands, Inc.

US

Last updated May 25, 2026

What Naturalena Brands, Inc. makes

Naturalena Brands, Inc. manufactures unscented menstrual tampons and pads, designed for personal hygiene during menstruation. The products are marketed under the Veeda brand and are intended for internal and external use depending on the device type.

The company’s portfolio includes devices classified as Class I and Class II under US regulations, with some products listed via FDA’s 510(k) and UDI programs. These products are based in the United States and comply with applicable regulatory requirements for menstrual hygiene products.

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 Naturalena Brands, Inc. manufacture?

Naturalena Brands, Inc. specializes in menstrual hygiene products, specifically unscented menstrual tampons and pads. These devices are designed for internal (tampons) and external (pads) use during menstruation, focusing on personal comfort and hygiene.

Where is Naturalena Brands, Inc. based, and what regulatory framework does it follow?

Naturalena Brands, Inc. is based in the United States. Its devices fall under US regulatory classification, including Class I and Class II categories, which determine the level of oversight required for safety and performance. The company ensures compliance with applicable US regulations for menstrual hygiene products.

Which regulatory registries or databases list Naturalena Brands, Inc.’s devices?

Naturalena Brands, Inc.’s devices are listed in the FDA’s 510(k) premarket notification program and the FDA’s Unique Device Identification (UDI) system. These registries help track and verify the compliance and classification of its products under US medical device regulations.

How are Naturalena Brands, Inc.’s devices classified under US regulations?

Naturalena Brands, Inc.’s devices are classified as either Class I or Class II under the US Food and Drug Administration’s regulatory framework. Class I generally includes low-risk devices requiring general controls, while Class II involves additional performance standards or special controls to ensure safety and effectiveness, depending on the specific product.

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
047756618

Catalogue (16)

DeviceModel / ReferenceRegistriesClassStatus
Veeda VDTSP32US
FDA UDI
Class IIActive
Veeda VATR90US
FDA UDI
Class IIActive
Veeda VPLFO40US
FDA UDI
Class IActive
Veeda VDTS16US
FDA UDI
Class IIActive
Veeda VATS90US
FDA UDI
Class IIActive
Veeda VATR16US
FDA UDI
Class IIActive
Veeda VPRW14US
FDA UDI
Class IActive
Veeda VDTS32US
FDA UDI
Class IIActive
Veeda VDTR16US
FDA UDI
Class IIActive
Veeda VDTSP16US
FDA UDI
Class IIActive
Veeda VDTR32US
FDA UDI
Class IIActive
Veeda VATS16US
FDA UDI
Class IIActive
Veeda VATSP16US
FDA UDI
Class IIActive
Veeda VATL16US
FDA UDI
Class IIActive
Veeda VPRN12US
FDA UDI
Class IActive
Veeda 100% Cotton Menstrual Tampon K130609
FDA 510(k)
Class IIActive

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