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Maquet, Inc.

US

Last updated May 24, 2026

Part of Maquet Sas

What Maquet, Inc. makes

Maquet, Inc. manufactures components and accessories for surgical and examination tables, including reusable headrests, orthopaedic extensions, leg and arm positioners, and medical table clamps. Their portfolio also includes specialized modules like padded urology plates, femur hooks, shoulder supports, and counter traction posts, as well as universal remote controls for operating room equipment. The company produces both reusable and disposable components tailored for surgical procedures and patient positioning.

The devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Maquet, Inc. is based in the United States, where these products are regulated under applicable medical device laws.

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 Maquet, Inc. manufacture?

Maquet, Inc. specializes in components and accessories designed for surgical and examination tables. Their products include reusable and disposable items such as operating table top extensions, orthopaedic positioners (like leg and arm supports), reusable headrests, medical table clamps, and specialized modules such as padded urology plates, femur hooks, and shoulder modules. These devices are tailored to enhance patient positioning and procedural efficiency in operating rooms.

Where is Maquet, Inc. based, and how does that affect its devices?

Maquet, Inc. is headquartered in the United States, where its medical devices are subject to FDA regulations. Since the company operates within the US, its products must comply with FDA requirements, including classification under Class I or Class II categories and registration in the FDA’s Unique Device Identifier (UDI) database. This ensures traceability and adherence to US medical device standards.

Which regulatory registries list Maquet, Inc.’s devices?

Maquet, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product identifier to medical devices, enabling better tracking, monitoring, and regulatory oversight. This listing helps healthcare providers and regulators verify the identity and compliance status of the company’s products.

How are Maquet, Inc.’s devices classified under FDA regulations?

Maquet, Inc.’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with, as outlined in FDA guidelines.

What is the purpose of the reusable and disposable components Maquet, Inc. produces?

Maquet, Inc. designs both reusable and disposable components to address different clinical needs. Reusable items like headrests, orthopaedic extensions, and arm positioners are engineered for durability and repeated use in surgical settings, reducing waste and costs. Disposable components, such as certain pads or modules, are intended for single-use procedures to ensure hygiene and minimize cross-contamination risks, aligning with infection control protocols in healthcare environments.

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

Information

Country
US
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Catalogue (962)

Page 6 of 20
DeviceModel / ReferenceRegistriesClassStatus
Powerled Tm ARD568420051A
FDA UDI
Class IIUnknown
MAGNUS operating table system 118001B4
FDA UDI
Class IActive
Standop Volista® ARDSAT209037A
FDA UDI
Class IIUnknown
Standop Volista® ARDVST229016A
FDA UDI
Class IIUnknown
Powerled Tm ARD568446751A
FDA UDI
Class IIUnknown
Standop Volista® ARDVST229017A
FDA UDI
Class IIUnknown
Powerled Tm ARD515011931A
FDA UDI
Class IIUnknown
Powerled Tm ARD568431755A
FDA UDI
Class IIUnknown
Pelvis plate 141905C0
FDA UDI
Class IActive
Extension plate 113131FC
FDA UDI
Class IActive
Maquet PowerLED II ARDPWT259281A
FDA UDI
Class IIUnknown
MAGNUS operating table system 118001D0
FDA UDI
Class IActive
Back plate 118031F0
FDA UDI
Class IActive
Head rest 118053A0
FDA UDI
Class IActive
CORIN mobile operating table 770001B0
FDA UDI
Class IActive
Corded control device 720090A0
FDA UDI
Class IActive
Transfer board 113265A0
FDA UDI
Class IActive
Fixture for body supports 100219C0
FDA UDI
Class IActive
Standop Volista® ARDSAT209033A
FDA UDI
Class IIUnknown
Standop Volista® ARDVST229034A
FDA UDI
Class IIUnknown
Powerled Tm ARD568441252A
FDA UDI
Class IIUnknown
Powerled Tm ARD267800350A
FDA UDI
Class IIUnknown
Lucea Led® ARDLCA209016A
FDA UDI
Class IIUnknown
Rectal positioning device 113056A0
FDA UDI
Class IActive
Powerled Tm ARD568446252A
FDA UDI
Class IIUnknown
Traction set 100366A0
FDA UDI
Class IActive
Foot switch 100981E3
FDA UDI
Class IActive
Powerled Tm ARDPWD209009A
FDA UDI
Class IIUnknown
Standop Volista® ARDVST229027A
FDA UDI
Class IIUnknown
Back/buttocks support 100211A0
FDA UDI
Class IActive
Head rest adapter 100716A0
FDA UDI
Class IActive
TRIMANO FORTIS Support Arm 100230R0
FDA UDI
Class IActive
Powerled Tm ARD568431251A
FDA UDI
Class IIUnknown
Volista Access ARDVCS209005A
FDA UDI
Class IIUnknown
MAGNUS operating table system 118001B1
FDA UDI
Class IActive
Powerled Tm ARDROL309030A
FDA UDI
Class IIUnknown
Powerled Tm ARD268400140A
FDA UDI
Class IIUnknown
Powerled Tm ARD568431053A
FDA UDI
Class IIUnknown
Transmobil TT-M 607342A0
FDA UDI
Class IIActive
Pad 10037400
FDA UDI
Class IActive
Powerled Tm ARD568411753A
FDA UDI
Class IIUnknown
Powerled Tm ARD568424513A
FDA UDI
Class IIUnknown
Powerled Tm ARD568424753A
FDA UDI
Class IIUnknown
Transporter 118065B0
FDA UDI
Class IActive
Adapter for uni-frame MAGNUS 100727A0
FDA UDI
Class IActive
Powerled Tm ARDPWD209042A
FDA UDI
Class IIUnknown
Pair of leg plates 100742AC
FDA UDI
Class IActive
Powerled Tm ARD568411251A
FDA UDI
Class IIUnknown
Support arm 10055800
FDA UDI
Class IActive
Head rest 113064F0
FDA UDI
Class IActive

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