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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 14 of 24
DeviceModel / ReferenceRegistriesClassStatus
Freedom Bath AF14004US10
FDA UDI
Class IIActive
Symbliss Bath SBS050US01
FDA UDI
Class IIActive
AtmosAir Velaris 633017
FDA UDI
Class IIActive
Primo AP03811US0001
FDA UDI
Class IIActive
Rhapsody AR01312US0011
FDA UDI
Class IIActive
Primo AP31801US2000
FDA UDI
Class IIActive
Citadel Plus FXX11A1B3AMABA
FDA UDI
Class IIActive
Nimbus 650201EVE
FDA UDI
Class IIActive
Citadel CX612B3K4AMAD0
FDA UDI
Class IIActive
Primo Ferro AS33212-US
FDA UDI
Class IIActive
Symbliss Bath SBL060US00
FDA UDI
Class IIActive
Primo AP32211US1100
FDA UDI
Class IIActive
Citadel CX712B3J4AMAD0
FDA UDI
Class IIActive
Harmony Bath AD31800US1010
FDA UDI
Class IIActive
Primo AP33801US2011
FDA UDI
Class IIActive
Tornado FA7E031120DUS1
FDA UDI
Class IActive
Primo AP32202US1010
FDA UDI
Class IIActive
Citadel CX811B3F4AMAB1
FDA UDI
Class IIActive
Freedom Bath AF14000US00
FDA UDI
Class IIActive
Primo AP32211US1001
FDA UDI
Class IIActive
AtmosAir Velaris 633902
FDA UDI
Class IIActive
Primo AP05811US10100
FDA UDI
Class IIActive
Arjo Slides Tube NPA0700
FDA UDI
Class IActive
Enterprise 9812CF111BCUSB
FDA UDI
Class IIActive
Harmony Bath AD31811US0010
FDA UDI
Class IIActive
Rhapsody AR02211US2000
FDA UDI
Class IIActive
Rhapsody AR02211US2101
FDA UDI
Class IIActive
Arjo Slides Tube NPA0750
FDA UDI
Class IActive
Maxi Sky 2 MS035
FDA UDI
Class IActive
Symbliss Bath SBL050US00
FDA UDI
Class IIActive
Primo AP32311US0111
FDA UDI
Class IIActive
Primo AP31202US2011
FDA UDI
Class IIActive
Symbliss Bath SBS030US01
FDA UDI
Class IIActive
Arjo Slides Tube NSA0900
FDA UDI
Class IActive
Harmony Bath AD33312US1011
FDA UDI
Class IIActive
Freedom Bath AF14004US01
FDA UDI
Class IIActive
Freedom Bath AF24004US10
FDA UDI
Class IIActive
Arjo Sling MAA1152-L
FDA UDI
Class IActive
Symbliss Bath SBL011US01
FDA UDI
Class IIActive
Freedom Bath AF24024US11
FDA UDI
Class IIActive
AtmosAir Velaris 633047
FDA UDI
Class IIActive
Rik PPO3001
FDA UDI
Class IActive
Primo AP32211US2111
FDA UDI
Class IIActive
Flowtron FG100S
FDA UDI
Class IIUnknown
Harmony Bath AD33212US1010
FDA UDI
Class IIActive
Maxi Sky 2 MS111
FDA UDI
Class IActive
Auralis 636T01N-P
FDA UDI
Class IIActive
Citadel CX711B2F3AMAB0
FDA UDI
Class IIActive
Maxi Sky 2 MS122
FDA UDI
Class IActive
Primo AP03312US0011
FDA UDI
Class IIActive

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