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IntelliGuard Group, LLC

US

Last updated May 31, 2026

What IntelliGuard Group, LLC makes

IntelliGuard Group, LLC manufactures anesthesia cabinets designed for use in surgical and procedural settings, including the IntelliGuard® Anesthesia system. These devices are engineered to deliver controlled gas mixtures and monitor anesthesia delivery parameters within operating rooms and clinical environments.

The company’s products fall under FDA Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 IntelliGuard Group, LLC primarily manufacture?

IntelliGuard Group, LLC specializes in anesthesia cabinets, such as the IntelliGuard® Anesthesia system. These devices are specifically designed for surgical and procedural settings to deliver controlled gas mixtures and monitor anesthesia delivery parameters in operating rooms and clinical environments.

Where is IntelliGuard Group, LLC based?

IntelliGuard Group, LLC is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device standards.

Which regulatory registries or databases list IntelliGuard Group, LLC’s devices?

IntelliGuard Group, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance with regulatory requirements.

How are IntelliGuard Group, LLC’s devices classified under FDA regulations?

IntelliGuard Group, LLC’s devices fall under FDA Class I classification. This classification is typically assigned to low-risk medical devices, such as anesthesia cabinets, where the risk of illness or injury is minimal. The classification determines the regulatory pathway and oversight required for authorization.

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
963409581

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
IntelliGuard® Anesthesia 5700-AS
FDA UDI
Class IActive

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