Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Prime Life Fibers Inc.

United States·US-MF-000014613

Last updated September 18, 2026

About

Wearever Incontinence is your source for reusable washable incontinence products for men and women.

From the manufacturer's own website. Source

What Prime Life Fibers Inc. makes

Prime Life Fibers Inc. manufactures reusable incontinence pants designed for both men and women, focusing on washable and disposable alternatives for bladder control needs.

These products fall under Class I medical devices and are registered in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. The company 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 Prime Life Fibers Inc. manufacture?

Prime Life Fibers Inc. specializes in reusable incontinence pants. These products are designed as washable alternatives to disposable incontinence solutions, catering to both men and women who require bladder control assistance. The focus is on providing a sustainable option for managing incontinence.

Where is Prime Life Fibers Inc. based?

Prime Life Fibers Inc. is headquartered in the United States. The company’s location influences its regulatory compliance, particularly for devices marketed in the US and EU, where its products are registered.

Which regulatory registries list Prime Life Fibers Inc.’s devices?

Prime Life Fibers Inc.’s devices are listed in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. These registries ensure transparency and traceability of medical devices in their respective markets, helping healthcare providers and regulators verify compliance.

How are Prime Life Fibers Inc.’s incontinence pants classified under medical device regulations?

Prime Life Fibers Inc.’s reusable incontinence pants fall under Class I medical device classification. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, such as certain personal care and protective items. Class I devices often require fewer regulatory controls but still must meet basic safety and performance standards.

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

Information

Country
United States
Address
4537 Hillsborough Road, DURHAM, United States
LinkedIn
—
Facebook
—
Phone
9194774400
PRRC Contact
Robert Deerin
EUDAMED SRN
US-MF-000014613
FDA FEI Number
—
DUNS Number
—

Catalogue (24)

DeviceModel / ReferenceRegistriesClassStatus
Hdl600bgemd HDL600BGEMD
EUDAMED
Class IActive
Wearever MBB300-NAV-3X-EA
FDA UDI
Class IActive
Wearever MBB300-NAV-MD-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-1X-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-2X-EA
FDA UDI
Class IActive
Wearever MBB300-GRY-LG-EA
FDA UDI
Class IActive
Wearever MBB300-NAV-2X-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-SM-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-3X-EA
FDA UDI
Class IActive
Wearever MBB300-GRY-SM-EA
FDA UDI
Class IActive
Wearever MBB300-GRY-2X-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-SM-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-1X-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-MD-EA
FDA UDI
Class IActive
Wearever MBB300-NAV-1X-EA
FDA UDI
Class IActive
Wearever MBB300-NAV-LG-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-MD-EA
FDA UDI
Class IActive
Wearever MBB300-NAV-SM-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-LG-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-LG-EA
FDA UDI
Class IActive
Wearever HDL600-BLK-3X-EA
FDA UDI
Class IActive
Wearever MBB300-GRY-3X-EA
FDA UDI
Class IActive
Wearever MBB300-WHT-2X-EA
FDA UDI
Class IActive
Wearever MBB300-GRY-1X-EA
EUDAMEDFDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.