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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

Country
US
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Catalogue (1172)

Page 2 of 24
DeviceModel / ReferenceRegistriesClassStatus
Symbliss Bath SBL061US01
FDA UDI
Class IIActive
Arjo Sling MFA1000M-L
FDA UDI
Class IActive
Citadel CX611B1F1AMAB0
FDA UDI
Class IIActive
AtmosAir 9000X 633034
FDA UDI
Class IActive
Primo Ferro AS32312US0110
FDA UDI
Class IIActive
Primo AP33801US1010
FDA UDI
Class IIActive
Airpal AP-050SPSS-DR
FDA UDI
Class IActive
Maxi Move 5 KMEHEU-0
FDA UDI
Class IActive
Arjo Sling MAA7090M-M
FDA UDI
Class IActive
Skin Iq 1000 SIQCPBAS1US
FDA UDI
Class IIActive
Primo AP32212US1001
FDA UDI
Class IIActive
Carevo BAC1101-01
FDA UDI
Class IActive
Citadel CX812A3K1AMAD0
FDA UDI
Class IIActive
Primo Ferro AS33312US0011
FDA UDI
Class IIActive
Primo AP32212US2001
FDA UDI
Class IIActive
Harmony Bath AD31800US0010
FDA UDI
Class IIActive
Primo AP32212US1110
FDA UDI
Class IIActive
Primo AP01212US1010
FDA UDI
Class IIActive
Primo AP31212US1000
FDA UDI
Class IIActive
Primo AP02811US1001
FDA UDI
Class IIActive
Rhapsody AR32212US1111
FDA UDI
Class IIActive
Tornado FA7B031120DUS1
FDA UDI
Class IActive
Citadel Plus FX611B1B1AMABA
FDA UDI
Class IIActive
Primo AP32212US2101
FDA UDI
Class IIActive
Flowtron Acs800 513003-P
FDA UDI
Class IIUnknown
Primo AP33801US2000
FDA UDI
Class IIActive
Primo AP32212US1101
FDA UDI
Class IIActive
Enterprise 9813BF101BGUSB
FDA UDI
Class IIActive
Arjo Sling MFA2100-M
FDA UDI
Class IActive
Flowtron Acs900 526000-02
FDA UDI
Class IIActive
Freedom Bath AF21104US11
FDA UDI
Class IIActive
Autologic PXB005ADV
FDA UDI
Class IIActive
Maxi Sky 2 MS000
FDA UDI
Class IActive
Enterprise 9712DC101ADUSB
FDA UDI
Class IIActive
Primo AP33811US1011
FDA UDI
Class IIActive
Symbliss Bath SBL020US00
FDA UDI
Class IIActive
Symbliss Bath SBS061US01
FDA UDI
Class IIActive
Parker Bath AL27010-US
FDA UDI
Class IIActive
Airpal AP-028SPSLH
FDA UDI
Class IActive
Sara Plus HEP0001-US
FDA UDI
Class IActive
Skin Iq 1000 SIQCOBAS1UN
EUDAMEDFDA UDI
Class IIActive
Arjo Sling THA6I-XS-33
FDA UDI
Class IActive
Maxi Move KMCSXN
FDA UDI
Class IActive
Primo AP32811US2001
FDA UDI
Class IIActive
Enterprise 9812HF111BCUSB
FDA UDI
Class IIActive
Primo AP33202US0011
FDA UDI
Class IIActive
Concerto BAB1103-01
FDA UDI
Class IActive
Freedom Bath AF11104US11
FDA UDI
Class IIActive
Maxi Move KMCEXN
FDA UDI
Class IActive
Harmony Bath AD32811US1000
FDA UDI
Class IIActive

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