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Arjohuntleigh, Inc.

US

Last updated May 24, 2026

Part of Arjohuntleigh AB

What Arjohuntleigh, Inc. makes

Arjohuntleigh manufactures patient mobility and bathing solutions, including electrically-powered mobile lifting systems, basic and bariatric hospital beds, and alternating-pressure mattress overlays. Their product line also covers hydrotherapy baths and walk-in bathtubs designed for accessibility, as well as general-purpose and specialized patient lifting slings, harnesses, and stretchers. The company produces sliding sheets and other assistive devices to aid patient transfer and positioning in clinical settings.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in hospitals, rehabilitation centers, and home care environments, adhering to regulatory standards for medical devices 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 Arjohuntleigh, Inc. manufacture?

Arjohuntleigh, Inc. specializes in patient mobility and bathing solutions. Their product line includes electrically-powered mobile patient lifting systems, basic and bariatric hospital beds, alternating-pressure mattress overlays, hydrotherapy baths, and walk-in bathtubs. They also produce general-purpose and specialized patient lifting slings, harnesses, and stretchers, as well as assistive devices like sliding sheets to aid patient transfers and positioning in clinical settings.

Where is Arjohuntleigh, Inc. based?

Arjohuntleigh, Inc. is headquartered in the United States. The company designs and manufactures its devices with a focus on meeting regulatory requirements for medical equipment in the U.S. market.

Which regulatory registries list Arjohuntleigh’s devices?

Arjohuntleigh’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, allowing them to verify and track the devices in use. The UDI system is a key resource for compliance and device identification in the U.S.

How are Arjohuntleigh’s devices classified under FDA regulations?

Arjohuntleigh’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards due to moderate risk. The classification depends on factors like the device’s intended use, potential harm, and complexity, ensuring appropriate regulatory oversight.

What environments are Arjohuntleigh’s devices intended for?

Arjohuntleigh’s devices are designed for use in hospitals, rehabilitation centers, and home care settings. Their products address mobility, bathing accessibility, and patient transfer needs, aligning with clinical environments where patient safety and comfort are prioritized. The range includes both institutional-grade equipment and solutions for home use.

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

Information

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US
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Catalogue (1172)

Page 12 of 24
DeviceModel / ReferenceRegistriesClassStatus
Skin Iq 365 SIQFNRU04UN
FDA UDI
Class IIActive
Autologic PXA001DAR
FDA UDI
Class IIActive
Arjo Sling MAA4160M-M
FDA UDI
Class IActive
Typhoon SA3H11B11AUS1
FDA UDI
Class IActive
Primo Ferro AS52302US0110
FDA UDI
Class IIActive
Maxi Move KMCSXE
FDA UDI
Class IActive
Arjo Sling 626002C-M
FDA UDI
Class IActive
Symbliss SYBCB001-US
FDA UDI
Class IActive
Enterprise 9613BF111BCUSB
FDA UDI
Class IIActive
Citadel CX711A2F2AMABA1
FDA UDI
Class IIActive
Harmony Bath AD31801US2000
FDA UDI
Class IIActive
Evenda EN21AFD0ASQAACA
FDA UDI
Class IIActive
Symbliss Bath SBL041US01
FDA UDI
Class IIActive
Alpha Trancell Deluxe ALT03
FDA UDI
Class IIActive
Enterprise 9612CF101BCUSB
FDA UDI
Class IIActive
Rhapsody AR02211US2010
FDA UDI
Class IIActive
Maxi 500 KM560100
FDA UDI
Class IActive
Enterprise 9814DF111BCUSB
FDA UDI
Class IIActive
Calypso CDB6023-01
FDA UDI
Class IActive
Citadel CX712B2J3AMAD0
FDA UDI
Class IIActive
Citadel CX811A1F1ACAA0
FDA UDI
Class IIActive
Primo AP32212US2011
FDA UDI
Class IIActive
Primo AP32212US1010
FDA UDI
Class IIActive
Primo AP32211US2010
FDA UDI
Class IIActive
Tornado FA3E031010AUS1
FDA UDI
Class IActive
Enterprise 9815A2111BCUSD
FDA UDI
Class IIActive
Primo AP33202US2011
FDA UDI
Class IIActive
Rhapsody AR02211US0000
FDA UDI
Class IIActive
Rhapsody AR02211US1010
FDA UDI
Class IIActive
Primo AP03811US2011
FDA UDI
Class IIActive
Rhapsody AR02211US1111
FDA UDI
Class IIActive
Citadel CX81B3F4AMAB0
FDA UDI
Class IIActive
Bolero CEB6023-01
FDA UDI
Class IActive
AtmosAir Velaris 633019
FDA UDI
Class IIActive
Symbliss Bath SBS021US00
FDA UDI
Class IIActive
Flowtron L503-M
FDA UDI
Class IIActive
Enterprise 9811DF101BGUSB
FDA UDI
Class IIActive
Harmony Bath AD33811US1000
FDA UDI
Class IIActive
Primo AP31811US0001
FDA UDI
Class IIActive
Citadel CX812B3J4AMAD0
FDA UDI
Class IIActive
Primo Ferro AS52202US0010
FDA UDI
Class IIActive
Maxi Move KMCEUN
FDA UDI
Class IActive
Primo AP31801US1000
FDA UDI
Class IIActive
Primo AP32212US0001
FDA UDI
Class IIActive
Enterprise 9714EF111BCUSB
FDA UDI
Class IIActive
Primo AP31811US1010
FDA UDI
Class IIActive
FirstStep Select 203660
FDA UDI
Class IIActive
Minuet 2 160AN2A1U
FDA UDI
Class IIActive
Arjo Slides Sheet NPAV5000
FDA UDI
Class IActive
Arjo Sling MAA4160M-XL
FDA UDI
Class IActive

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