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TALON

US

Last updated May 31, 2026

What TALON makes

The company produces vacuum-mould patient positioning systems designed to secure and immobilize patients during medical procedures, ensuring stability and reducing repositioning risks. Their product line includes the VacFix Pump, which likely integrates with vacuum-mould systems to enhance patient support and procedural efficiency.

These devices are classified as Class I under regulatory frameworks, indicating low-risk medical equipment. They are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements. The company operates from 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 Talon manufacture?

Talon specializes in vacuum-mould patient positioning systems, which are designed to secure and immobilize patients during medical procedures. These systems help maintain stability and minimize the need for repositioning, improving safety and efficiency. An example of their product is the VacFix Pump, which likely works alongside vacuum-mould systems to enhance patient support.

Where is Talon based, and what regulatory region does it operate in?

Talon is based in the United States. Their devices are developed and marketed within the U.S. regulatory framework, ensuring compliance with local standards for medical equipment.

Which regulatory registries or databases list Talon’s devices?

Talon’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices in the U.S., ensuring transparency and traceability for regulatory and clinical purposes.

How are Talon’s devices classified under regulatory standards?

Talon’s devices fall under Class I classification, which is the lowest risk category for medical equipment under regulatory frameworks. This classification is assigned based on factors like the device’s purpose, intended use, and potential risks, indicating they pose minimal risk to patients when used as directed.

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

Information

Country
US
Address
—
LinkedIn
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Facebook
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Phone
2818151300
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
005574330

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
VacFix Pump VF-PUMP
FDA UDI
Class IActive

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