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Iron Duck Inc

United States·US-MF-000016043

Last updated September 18, 2026

What Iron Duck Inc makes

Iron Duck Inc manufactures spinal immobilization devices, including rigid spineboards and specialized variants like the Ultra Vue and Ultra Space Save series, designed for prehospital and emergency medical use. These products are intended for patient transport and stabilization to protect the spine during movement. The company also produces Boxmet spineboards, which are likely constructed from composite materials for durability and lightweight transport.

The company’s products are classified as Class I medical devices under EU regulations and are registered in the EUDAQMED database. While the devices are listed in eudamed, regulatory classification and compliance are determined on a per-device basis. 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 Iron Duck Inc manufacture?

Iron Duck Inc specializes in spinal immobilization devices, including rigid spineboards and specialized variants like the Ultra Vue (e.g., Ultra Vue 18 - 35755YP and Ultra Vue 16 - 35775YP), Ultra Space Save (e.g., Ultra Space Save – 35940), and Boxmet spineboards. These products are designed for prehospital and emergency medical use to stabilize and protect the spine during patient transport.

Where is Iron Duck Inc based?

Iron Duck Inc is based in the United States. While the company’s headquarters location is not specified, its regulatory filings and device listings reflect a US origin.

Which regulatory registries list Iron Duck Inc’s devices?

Iron Duck Inc’s devices are listed in the EUDAQMED database, which is the official European database for medical devices. This registry tracks devices that have undergone regulatory processes, such as classification and conformity assessment, under EU regulations.

How are Iron Duck Inc’s devices classified under EU regulations?

Iron Duck Inc’s devices are classified as Class I medical devices under EU regulations. This classification applies to low-risk products like spinal immobilization devices, which typically require general safety and performance requirements but may not need additional pre-market authorization steps beyond manufacturer declaration.

Are Iron Duck Inc’s devices authorized for use in the EU?

Iron Duck Inc’s devices are registered in eudamed, meaning they have been classified and, where applicable, have undergone conformity assessment procedures (e.g., EU Declaration of Conformity) to demonstrate compliance with EU Medical Device Regulations (MDR) or previous directives. However, authorization for use depends on individual devices meeting regulatory requirements, not the company itself.

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

Information

Country
United States
Address
—
Phone
413-593-3300
PRRC Contact
Mike Fleming
EUDAMED SRN
US-MF-000016043
FDA FEI Number
—
DUNS Number
—

Catalogue (8)

DeviceModel / ReferenceRegistriesClassStatus
Lifeguard Spineboard Lifeguard Spineboard mit Speed-Clip ohne Gurte, Schwarz
EUDAMED
Class IActive
Lifeguard Spineboard Lifeguard spineboard mit Speed-Clip Pin ohne Gurte, olivegrune
EUDAMED
Class IActive
Lifeguard Spineboard Lifeguard Spineboard mlt Speed-Clip ohne Gurte, gelb
EUDAMED
Class IActive
Ultra Vue 18 - 35755YP Ultra Vue 18 - 35755YP
EUDAMED
Class IActive
Boxmet Spine borads Boxmet 35775-YP
EUDAMED
Class IActive
Ultra Vue 16 - 35775YP Ultra Vue 16 - 35775YP
EUDAMED
Class IActive
Lifeguard Spineboard Lifeguard Spineboard, gelb, ohne Fixiergurte-N5 0100Y
EUDAMED
Class IActive
Ultra Space Save – 35940 Ultra Space Save – 35940
EUDAMED
Class IActive

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