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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 16 of 24
DeviceModel / ReferenceRegistriesClassStatus
Primo Ferro AS32202-US
FDA UDI
Class IIActive
Arjo Sling MAA4080M-L
FDA UDI
Class IActive
Symbliss Bath SBL020US01
FDA UDI
Class IIActive
AtmosAir Velaris 633046
FDA UDI
Class IIActive
Arjo Slides Tube NSA0600
FDA UDI
Class IActive
Primo AP03312US1010
FDA UDI
Class IIActive
Primo AP31202US0000
FDA UDI
Class IIActive
Autologic PXB001DAR
FDA UDI
Class IIActive
Primo AP32212US0101
FDA UDI
Class IIActive
Primo AP02211US2111
FDA UDI
Class IIActive
Freedom Bath AF24020US01
FDA UDI
Class IIActive
Primo AP31202US0001
FDA UDI
Class IIActive
AtmosAir Velaris 633016
FDA UDI
Class IIActive
Flowtron DVT30S
FDA UDI
Class IIUnknown
Flowtron Tri Pulse TRP30
FDA UDI
Class IIActive
Primo AP33311US1010
FDA UDI
Class IIActive
Citadel CX812B1J1AMAD0
FDA UDI
Class IIActive
Maxi Air MAS16000-US
FDA UDI
Class IActive
Enterprise 9711AF111BCUSB
FDA UDI
Class IIActive
AtmosAir T-Series AR
FDA UDI
Class IIActive
Primo AP35811US20100
FDA UDI
Class IIActive
Primo AP31212US2001
FDA UDI
Class IIActive
Symbliss Bath SBS011US01
FDA UDI
Class IIActive
Rhapsody AR02211US0010
FDA UDI
Class IIActive
Enterprise 9811CF101BGUSB
FDA UDI
Class IIActive
Enterprise 9714DF101BCUSB
FDA UDI
Class IIActive
Primo AP33212US1011
FDA UDI
Class IIActive
Primo AP02211US2000
FDA UDI
Class IIActive
Primo AP32211US0010
FDA UDI
Class IIActive
Primo AP33202US1011
FDA UDI
Class IIActive
Maxi Move KMCEXN-D
FDA UDI
Class IActive
Maxi Sky 440 LE00009
FDA UDI
Class IActive
Symbliss Bath SBS031US00
FDA UDI
Class IIActive
Harmony Bath AD32811US1011
FDA UDI
Class IIActive
Sara Flex HEB1000
FDA UDI
Class IActive
Primo AP03811US1000
FDA UDI
Class IIActive
Citadel CX812B2J3AMAD0
FDA UDI
Class IIActive
Harmony Bath AD32801US1000
FDA UDI
Class IIActive
Harmony Bath AD36811US10100
FDA UDI
Class IIActive
Symbliss Bath SBL021US01
FDA UDI
Class IIActive
Flowtron Universal 507003OR
FDA UDI
Class IIUnknown
Citadel Plus FXX11C1D1ACABB
FDA UDI
Class IIActive
Primo Ferro AS32212US0101
FDA UDI
Class IIActive
Auralis 636M05SUS
FDA UDI
Class IIActive
Primo AP32211US1101
FDA UDI
Class IIActive
Parker Bath AL27016-US
FDA UDI
Class IIActive
Therarest TRMRLNB34078TEG
FDA UDI
Class IActive
Arjo Sling MAA4100M-LL
FDA UDI
Class IActive
AtmosAir 9000 AR
FDA UDI
Class IIActive
Citadel CX811A3E1AMAB0
FDA UDI
Class IIActive

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