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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 5 of 24
DeviceModel / ReferenceRegistriesClassStatus
Maxi Sky 1000 LF21000
FDA UDI
Class IActive
Citadel Plus FX611B3B4AMABB
FDA UDI
Class IIActive
Primo AP33811US0011
FDA UDI
Class IIActive
Maxi Sky 2 MS100-02
FDA UDI
Class IActive
Primo Ferro AS33801US0010
FDA UDI
Class IIActive
Harmony Bath AD31212US0010
FDA UDI
Class IIActive
Arjo Sling THAI-L-33
FDA UDI
Class IActive
Airpal AP-034SPS
FDA UDI
Class IActive
Autologic PXA001ADV
FDA UDI
Class IIActive
Arjo Sling 626003M
FDA UDI
Class IActive
Maxi Sky 2 MS400
FDA UDI
Class IActive
Maxi Move 5 KMESEU-M
FDA UDI
Class IActive
Primo AP32211US0101
FDA UDI
Class IIActive
Primo Ferro AS52312US0110
FDA UDI
Class IIActive
Harmony Bath AD31801US1011
FDA UDI
Class IIActive
Arjo Sling MAA4050M-L
FDA UDI
Class IActive
Primo AP31202US0011
FDA UDI
Class IIActive
Primo AP32212US1100
FDA UDI
Class IIActive
Concerto BAB3103-01
FDA UDI
Class IActive
AtmosAir Velaris 633027
FDA UDI
Class IIActive
Enterprise 9611AE101DCUSB
FDA UDI
Class IIActive
Harmony Bath AD33801US1010
FDA UDI
Class IIActive
Primo AP33312US2010
FDA UDI
Class IIActive
Harmony Bath AD33212US1011
FDA UDI
Class IIActive
Harmony Bath AD31212US0011
FDA UDI
Class IIActive
Primo AP31811US0010
FDA UDI
Class IIActive
Harmony Bath AD32811US0011
FDA UDI
Class IIActive
Freedom Bath AF24120US10
FDA UDI
Class IIActive
Symbliss Bath SBL061US00
FDA UDI
Class IIActive
Primo AP02211US1000
FDA UDI
Class IIActive
Skin Iq SIQCOSTS1UN
EUDAMEDFDA UDI
Class IIActive
Primo AP33801US0000
FDA UDI
Class IIActive
Primo AP02211US0011
FDA UDI
Class IIActive
Primo Ferro AS52302US0111
FDA UDI
Class IIActive
Airpal AP-050N
FDA UDI
Class IActive
Primo AP33811US0000
FDA UDI
Class IIActive
Multiclean BPA1100-US
FDA UDI
Class IActive
Harmony Bath AD32811US1001
FDA UDI
Class IIActive
Primo AP31811US1001
FDA UDI
Class IIActive
Citadel CX611B3F4AMAB1
FDA UDI
Class IIActive
AtmosAir Velaris 633003
FDA UDI
Class IIActive
Citadel Plus FXX11C3B4AMABB
FDA UDI
Class IIActive
Harmony Bath AD33202US1011
FDA UDI
Class IIActive
Freedom Bath AF21100US00
FDA UDI
Class IIActive
Symbliss Bath SBL021US00
FDA UDI
Class IIActive
AtmosAir Velaris 633044
FDA UDI
Class IIActive
Maxi Sky 2 MS010
FDA UDI
Class IActive
Primo AP02211US0000
FDA UDI
Class IIActive
Primo AP03311US0011
FDA UDI
Class IIActive
Arjo Slides Sheet NSAV5310
FDA UDI
Class IActive

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