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Trulife Inc.

United States·US-MF-000009657

Last updated September 17, 2026

About

Trulife is internationally based with over 60 years’ experience in the creation, development, manufacture of niche healthcare and consumer products.

From the manufacturer's own website. Source

What Trulife Inc. makes

Trulife Inc. manufactures mechanical-resistance external ankle-foot prostheses and knee cages. Their product offerings include the K2 Kinetic Foot with Pyramid.

The company is based in the United States, and its products are classified as Class I devices. These devices are listed in the EUDAMED database.

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 Trulife Inc. manufacture?

Trulife Inc. specializes in the production of mechanical-resistance external ankle-foot prostheses and knee cages. This information is based on the company's product summary, which identifies these specific categories as their primary manufacturing focus, including examples like the K2 Kinetic Foot with Pyramid.

Where is Trulife Inc. based?

Trulife Inc. is based in the United States. This location is confirmed by the company data provided, which specifies the United States as the country of origin for the manufacturer.

How are the devices from Trulife Inc. classified?

The devices manufactured by Trulife Inc. are classified as Class I. This classification is provided in the device data, which categorizes the company's product portfolio according to regulatory standards.

Which regulatory registries list Trulife Inc. devices?

Devices manufactured by Trulife Inc. are listed in the EUDAMED database. This registry is identified in the provided company data as the platform where their specific medical devices are recorded.

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

Information

Country
United States
Address
3225, Woburn St. Ste. 160, Bellingham WA., United States
LinkedIn
—
Facebook
—
Phone
+1 360 594 6177
PRRC Contact
Mike Sumner
EUDAMED SRN
US-MF-000009657
FDA FEI Number
3022549
DUNS Number
—

Catalogue (53)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
K1 Foot with Pyramid K1-K2 SCH113-28L
EUDAMED
Class IActive
Knee Cage 0866805
EUDAMED
Class IActive
Knee Cage 0866802
EUDAMED
Class IActive

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