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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 10 of 24
DeviceModel / ReferenceRegistriesClassStatus
Arjo Sling MFA1000M-M
FDA UDI
Class IActive
AtmosAir Velaris 633031
FDA UDI
Class IIActive
Primo AP03811US0010
FDA UDI
Class IIActive
Sara Combilizer APA1000-US
FDA UDI
Class IActive
Sara Plus KKA6000-M
FDA UDI
Class IActive
Primo AP01811US1010
FDA UDI
Class IIActive
Therarest TRMRLNB35080CHG
FDA UDI
Class IActive
Enterprise 9821DC101ADUSA
FDA UDI
Class IIActive
Enterprise 9812HP111BCUSB
FDA UDI
Class IIActive
Symbliss SYBCS011-US
FDA UDI
Class IActive
Autologic PXA201EVE
FDA UDI
Class IIActive
Maxi Sky 2 PLUS MS006-10
FDA UDI
Class IActive
Primo Ferro AS52302-US
FDA UDI
Class IIActive
Primo AP31801US2001
FDA UDI
Class IIActive
Freedom Bath AF21104-US
FDA UDI
Class IIActive
FirstStep Select 215200
FDA UDI
Class IIActive
Freedom Bath AF14124US10
FDA UDI
Class IIActive
Flowtron FG200
FDA UDI
Class IIActive
Primo AP33311US1011
FDA UDI
Class IIActive
Harmony Bath AD31811US2001
FDA UDI
Class IIActive
Primo AP31801US2010
FDA UDI
Class IIActive
Primo Ferro AS52212US0001
FDA UDI
Class IIActive
Citadel Plus FX811B3B4AMABA
FDA UDI
Class IIActive
Primo AP03212US1000
FDA UDI
Class IIActive
Harmony Bath AD32801US0001
FDA UDI
Class IIActive
Harmony Bath AD31811US0001
FDA UDI
Class IIActive
Freedom Bath AF14020US00
FDA UDI
Class IIActive
Primo Ferro AS33212US0001
FDA UDI
Class IIActive
Century AK63611-US
FDA UDI
Class IIActive
Enterprise 9813GF111BCUSB
FDA UDI
Class IIActive
Primo AP03212US1011
FDA UDI
Class IIActive
Primo AP32211US0100
FDA UDI
Class IIActive
AtmosAir 9000 A
FDA UDI
Class IIActive
Citadel Plus FX711B1B1AMABA
FDA UDI
Class IIActive
Harmony Bath AD31800US0011
FDA UDI
Class IIActive
Primo AP31801US0000
FDA UDI
Class IIActive
Carendo BIB2003-01
FDA UDI
Class IActive
Primo AP31801US1001
FDA UDI
Class IIActive
Primo AP02811US2001
FDA UDI
Class IIActive
Airpal AP-039SPSH
FDA UDI
Class IActive
Primo AP33811US2010
FDA UDI
Class IIActive
Citadel CX611A2F1ACAA0
FDA UDI
Class IIActive
Therarest TVMRLNB35080CHG
FDA UDI
Class IActive
Primo AP33202US1001
FDA UDI
Class IIActive
Primo Ferro AS32212US0110
FDA UDI
Class IIActive
Enterprise 9612BC101AFUSB
FDA UDI
Class IIActive
Primo AP32811US2000
FDA UDI
Class IIActive
Enterprise 9812DC101ADUSA
FDA UDI
Class IIActive
Primo AP33202US2010
FDA UDI
Class IIActive
Primo AP32312US0110
FDA UDI
Class IIActive

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