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Sign in to claim this brandJoerns Healthcare
US
Last updated September 17, 2026
About
Joerns is a leading partner in long-term post-acute care (LTPAC), providing access to high-quality products with renowned efficacy and safety
From the manufacturer's own website. Source
What Joerns Healthcare makes
Joerns Healthcare manufactures patient mobility and support devices, including general-purpose lifting slings and harnesses, basic electric hospital beds, and various mattress overlays such as alternating-pressure and low-air-loss systems. Their portfolio also includes reusable patient positioners, inflators for pressure-relief mattresses, and foam mattresses designed for clinical use. Accessories for these systems are also produced.
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. Joerns Healthcare is based 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 Joerns Healthcare primarily manufacture?
Joerns Healthcare specializes in patient mobility and support devices. Their most common products include general-purpose patient lifting slings and harnesses, basic electric hospital beds, and mattress systems like alternating-pressure overlays, low-air-loss mattresses, and inflators. They also produce reusable patient positioners and foam mattresses, along with accessories for these systems. These devices are designed to assist in patient care, mobility, and pressure relief in clinical settings.
Where is Joerns Healthcare based, and how does that affect its regulatory standing?
Joerns Healthcare is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies Joerns Healthcare’s products as either Class I or Class II, which determines the level of scrutiny and regulatory requirements for each device type. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls or performance standards.
Are Joerns Healthcare’s devices listed in any regulatory registries, and why does this matter?
Yes, Joerns Healthcare’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This matters because the UDI system ensures traceability and transparency in the medical device supply chain. Listing in the UDI database helps healthcare providers, regulators, and other stakeholders quickly identify and verify the specific devices in use, ensuring proper tracking for safety, recalls, and compliance purposes.
How are Joerns Healthcare’s devices classified by the FDA, and what does that classification mean?
Joerns Healthcare’s devices are classified under FDA’s Class I and Class II categories. Classification determines the regulatory pathway and oversight required for each device. Class I devices, typically low-risk items like some slings or basic accessories, are subject to general controls such as good manufacturing practices. Class II devices, which may include more complex systems like electric hospital beds or pressure-relief mattress overlays, require additional controls like performance standards or post-market surveillance to ensure safety and effectiveness.
Why might a healthcare provider need to check the regulatory classification of Joerns Healthcare’s devices?
Healthcare providers may need to verify the regulatory classification of Joerns Healthcare’s devices to ensure they meet the appropriate safety and performance standards for their intended use. For example, Class II devices often require more rigorous validation processes, which can impact procurement decisions, clinical workflows, and compliance with healthcare facility policies. Understanding the classification helps providers assess the level of oversight and documentation associated with each device, ensuring proper integration into patient care environments.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 2430 Whitehall Park Dr Ste 700, Charlotte, NC, 28273
- Website
- www.joerns.com/
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3012392312
- DUNS Number
- —
Catalogue (540)
Page 4 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Slings | 111-D-LS-510 | FDA UDI | Class I | Active |
| Slings | WECC-WECARE-RAH | FDA UDI | Class II | Active |
| Slings | NA25515 | FDA UDI | Class I | Active |
| Slings | NA1001 | FDA UDI | Class I | Active |
| Accessories | N104 | FDA UDI | Class II | Active |
| Apex | HPL402 | FDA UDI | Class I | Active |
| Accessories | N302AL | FDA UDI | Class II | Active |
| Accessories | N165 | FDA UDI | Class II | Active |
| Apex Lifts | HML400-70000 | FDA UDI | Class I | Active |
| Slings | NA26912 | FDA UDI | Class I | Active |
| Apex Lifts | C-HLA-2-50021 | FDA UDI | Class I | Active |
| Slings | NA1069 | FDA UDI | Class I | Active |
| Accessories | F17TMAL | FDA UDI | Class II | Active |
| Derma Therapy | DT-PAD-3850-EA | FDA UDI | Class I | Active |
| Slings | NA1008P | FDA UDI | Class I | Active |
| Accessories | N300AL | FDA UDI | Class II | Active |
| Arise | ARLAL-4280-M | FDA UDI | Class II | Active |
| Slings | NA13499N | FDA UDI | Class I | Active |
| WeCare Response Bed | PAN1000-FLEX-RIL | FDA UDI | Class II | Active |
| Slings | NA25506 | FDA UDI | Class I | Active |
| Hoyer Lift | HOY-4PTWSC-LP | FDA UDI | Class I | Active |
| ProMatt Plus | PMP-CBC | FDA UDI | Class II | Active |
| Slings | 70051 | FDA UDI | Class I | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3582NCOOJ-M | FDA UDI | Class II | Unknown |
| ProCair Plus | 222-3680 | FDA UDI | Class II | Active |
| PrevaMatt | PVAL-3584FLTM4SZP | FDA UDI | Class I | Active |
| Gel Foam | PVEN-3580FLNA2SZP | FDA UDI | Class I | Active |
| Apex Lifts | C-HLA-2-70011 | FDA UDI | Class I | Active |
| Joerns FlapCair LAL | FC-3680-M | FDA UDI | Class II | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3582OOOOJ-M | FDA UDI | Class II | Active |
| Apex Lifts | HML400-70051 | FDA UDI | Class I | Active |
| Apex Lifts | C-CB-L2 | FDA UDI | Class I | Active |
| Slings | NA1003P | FDA UDI | Class I | Active |
| Arise | 1000 | FDA UDI | Class II | Active |
| Accessories | F028 | FDA UDI | Class II | Active |
| Apex Lifts | C-HLA-112PLC | FDA UDI | Class I | Active |
| PrevaMatt | PVDE-4280FLNA2SZP | FDA UDI | Class I | Active |
| TxCair Plus | TXLAL-3684-M | FDA UDI | Class II | Active |
| PrevaMatt | PVCO-3584FLNA2SZP | FDA UDI | Class I | Active |
| Apex Lifts | C-HLA-2-70053 | FDA UDI | Class I | Active |
| WeCare Response Bed | WECC42-T-NM-HSR-AL | FDA UDI | Class II | Active |
| PrevaMatt | PVAL-4284FLNA4SZP | FDA UDI | Class I | Active |
| PrevaMatt | PVAL-4280FLTM4SZP | FDA UDI | Class I | Active |
| PrevaMatt | PVAL-3580FLTM4SZP | FDA UDI | Class I | Active |
| Slings | NA25705 | FDA UDI | Class I | Active |
| WeCare Response Bed | WECC-TRD-NM-HSR-AL | FDA UDI | Class II | Active |
| Slings | NA25623 | FDA UDI | Class I | Active |
| WeCare Response Bed | WECC-TRD-QO-QSR-BA | FDA UDI | Class II | Active |
| ProMatt Plus | PMPE3180SZBADT | FDA UDI | Class I | Active |
| WeCare Response Bed | WECC-TRD-QO-PVBA | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Joerns Healthcare has five FDA recall records, all initiated between January 6, 2006, and May 3, 2018, with all records marked as terminated. The recalls involved issues with connectors in P.R.O. Matt and ProCair Mattresses, potential failure of the Easy-Care Care-Lock feature on beds, an unapproved reduction in welds on mattress bases, and hydraulic jack problems in select Hoyer Patient Lifts.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 3, 2018 | Z-2033-2018 | — | terminated | Joerns Healthcare has identified a potential issue with some of the P.R.O. Matt and ProCair Mattresses. For the identified serial number range of P.R.O. Matt and ProCair Mattresses incorrect connectors (part #s 206-0401 & 206-0405) were provided by a Joerns supplier without the required internal shutoff valves, these shutoff valves prevent air from escaping from the mattress air cells. |
| May 3, 2018 | Z-2034-2018 | — | terminated | Joerns Healthcare has identified a potential issue with some of the P.R.O. Matt and ProCair Mattresses. For the identified serial number range of P.R.O. Matt and ProCair Mattresses incorrect connectors (part #s 206-0401 & 206-0405) were provided by a Joerns supplier without the required internal shutoff valves, these shutoff valves prevent air from escaping from the mattress air cells. |
| Sep 24, 2014 | Z-0151-2015 | — | terminated | The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (locked) pedal. |
| Feb 21, 2007 | Z-0727-2007 | — | terminated | Unapproved Design Change (by base supplier) consisting of a reduction in the number of mast-to-base welds (from four welds to two welds). |
| Jan 6, 2006 | Z-0904-06 | — | terminated | A field correction is being conducted on select models of Hoyer Patient Lifts because of hydraulic jack problems that have resulted in patient injury. The possibility exists that the mounting stud located in the bottom of the hydraulic jack could become loose allowing the jack to disengage from the mast of the lift. |