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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 3 of 24
DeviceModel / ReferenceRegistriesClassStatus
Citadel CXX11A1F1ACAA0
FDA UDI
Class IIActive
Harmony Bath AD32811US0010
FDA UDI
Class IIActive
Flowtron Tri Pulse TRP20
FDA UDI
Class IIActive
Symbliss Bath SBL050US01
FDA UDI
Class IIActive
Arjo Sling THAI-M-33
FDA UDI
Class IActive
Maxi Sky 440 LE00000
FDA UDI
Class IActive
Freedom Bath AF24024US01
FDA UDI
Class IIActive
Arjo Sling THA6I-XL-33
FDA UDI
Class IActive
Primo AP31811US2000
FDA UDI
Class IIActive
Freedom Bath AF14120US00
FDA UDI
Class IIActive
Calypso CDB7023-01
FDA UDI
Class IActive
Rhapsody AR02211US1011
FDA UDI
Class IIActive
Symbliss Bath SBS060US00
FDA UDI
Class IIActive
Nimbus 650001ADV
FDA UDI
Class IIActive
Primo AP02211US0010
FDA UDI
Class IIActive
Maxi Move KMCSUN
FDA UDI
Class IActive
Flowtron Tri Pulse TRP40
FDA UDI
Class IIActive
Primo AP32212US1011
FDA UDI
Class IIActive
Primo AP03811US2001
FDA UDI
Class IIActive
Freedom Bath AF24104US10
FDA UDI
Class IIActive
Enterprise 9811AF101BCUSB
FDA UDI
Class IIActive
Maxi Sky 2 MS011
FDA UDI
Class IActive
Arjo Sling MFA1000M-S
FDA UDI
Class IActive
Freedom Bath AF11000US00
FDA UDI
Class IIActive
Freedom Bath AF11100US01
FDA UDI
Class IIActive
Citadel CX811A3H1AMAB0
FDA UDI
Class IIActive
Freedom Bath AF24000US10
FDA UDI
Class IIActive
Primo AP31212US2010
FDA UDI
Class IIActive
Freedom Bath AF24124US01
FDA UDI
Class IIActive
Primo AP03212US0000
FDA UDI
Class IIActive
Arjo Sling MAA4070M-XL
FDA UDI
Class IActive
AtmosAir Velaris 633020
FDA UDI
Class IIActive
AtmosAir 9000X 633041
FDA UDI
Class IActive
Harmony Bath AD32801US2001
FDA UDI
Class IIActive
Freedom Bath AF21000US01
FDA UDI
Class IIActive
Primo AP32211US1111
FDA UDI
Class IIActive
Freedom Bath AF24020US10
FDA UDI
Class IIActive
Freedom Bath AF14024US00
FDA UDI
Class IIActive
Freedom Bath AF14120US10
FDA UDI
Class IIActive
Enterprise 9611AE101BCUSB
FDA UDI
Class IIActive
AtmosAir Velaris 633043
FDA UDI
Class IIActive
Citadel CX611B2F3AMAB0
FDA UDI
Class IIActive
Arjo Sling MFA1000M-XL
FDA UDI
Class IActive
Primo AP33311US0011
FDA UDI
Class IIActive
Primo Ferro AS32202US0111
FDA UDI
Class IIActive
Primo AP31202US2001
FDA UDI
Class IIActive
Arjo Sling TIR-S-33
FDA UDI
Class IActive
Parker Bath AL26015-US
FDA UDI
Class IIActive
Arjo Sling THAI-S-33
FDA UDI
Class IActive
Symbliss Bath SBS010US00
FDA UDI
Class IIActive

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