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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 19 of 24
DeviceModel / ReferenceRegistriesClassStatus
Symbliss Bath SBS010US01
FDA UDI
Class IIActive
Freedom Bath AF14024US10
FDA UDI
Class IIActive
Nimbus Professional 651001EVE
FDA UDI
Class IIActive
Primo Ferro AS32801US0000
FDA UDI
Class IIActive
Enterprise 9818D2111BCUSD
FDA UDI
Class IIActive
Airpal AP-039SPS
FDA UDI
Class IActive
Maxi Sky 2 MS015
FDA UDI
Class IActive
Primo AP32211US2110
FDA UDI
Class IIActive
Harmony Bath AD32312US0110
FDA UDI
Class IIActive
Miranti CEB8203-01
FDA UDI
Class IActive
Maxi Move KMCLXN
FDA UDI
Class IActive
Maxi Sky 2 MS010-01
FDA UDI
Class IActive
Symbliss Bath SBS020US00
FDA UDI
Class IIActive
Tornado FA7E012010DUS1
FDA UDI
Class IActive
AtmosAir Velaris 633045
FDA UDI
Class IIActive
Enterprise 9613GF111BCUSB
FDA UDI
Class IIActive
Primo AP33312US2011
FDA UDI
Class IIActive
Primo AP33312US1011
FDA UDI
Class IIActive
Primo AP33211US0010
FDA UDI
Class IIActive
Symbliss Bath SBL051US01
FDA UDI
Class IIActive
Citadel CX711B3F4AMAB1
FDA UDI
Class IIActive
Primo AP31212US2000
FDA UDI
Class IIActive
Symbliss Bath SBS070US01
FDA UDI
Class IIActive
Primo AP31202US1000
FDA UDI
Class IIActive
Primo Ferro AS32202US0100
FDA UDI
Class IIActive
Maxi Sky 2 MS112
FDA UDI
Class IActive
AtmosAir 9000X 633038
FDA UDI
Class IActive
Primo AP33811US1010
FDA UDI
Class IIActive
Enterprise 9814EF111BCUSB
FDA UDI
Class IIActive
Freedom Bath AF11104US01
FDA UDI
Class IIActive
Primo AP31212US1001
FDA UDI
Class IIActive
AtmosAir Velaris 633018
FDA UDI
Class IIActive
Primo AP33202US0010
FDA UDI
Class IIActive
Primo AP33811US2000
FDA UDI
Class IIActive
Maxi Sky 2 MS110
FDA UDI
Class IActive
Harmony Bath AD31801US1000
FDA UDI
Class IIActive
Primo AP02211US0111
FDA UDI
Class IIActive
Arjo Sling MAA4100M-S
FDA UDI
Class IActive
Bolero CEB6003-01
FDA UDI
Class IActive
Symbliss Bath SBL030US01
FDA UDI
Class IIActive
Miranti CEB8303-01
FDA UDI
Class IActive
Parker Bath AL26010-US
FDA UDI
Class IIActive
Primo AP31811US2010
FDA UDI
Class IIActive
Primo AP31800US0010
FDA UDI
Class IIActive
Citadel CX811A3E2AMAB0
FDA UDI
Class IIActive
Flowtron Acs800 513003OR-P
FDA UDI
Class IIUnknown
Maxi Sky 2 PLUS MS000-10
FDA UDI
Class IActive
Symbliss Bath SBS030US00
FDA UDI
Class IIActive
Primo Ferro AS32202US0101
FDA UDI
Class IIActive
Arjo Sling MAA4070M-M
FDA UDI
Class IActive

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