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World desk5 min

Are Exoskeletons Safe to Use? Common Risks and Precautions Explained

Exoskeleton safety depends on the device, wearer, task, fit and environment. Here are the risks, evidence limits and precautions for workplace and medical use.
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Exoskeletons are not universally safe or unsafe: they may reduce some physical demands, but can also add weight, restrict movement, shift strain to other body areas or create hazards in a particular task or setting. Safety depends on the device, its fit, the wearer, the work or care task, the environment and training.

What risks can an exoskeleton create?

An exoskeleton supports or assists parts of the body, but it does not make physical load disappear. It can redistribute forces, change how a person moves or affect the ability to respond to a hazard. The risks below are possibilities identified in workplace guidance and studies; they do not mean every wearer will experience them.

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Strain, pressure and nerve effects

NIOSH’s industrial guidance warns that a powered device could move a joint beyond its normal range and contribute to muscle strain. Added device weight or load shifted to another body area can create a different physical demand instead of removing one. Pressure from prolonged wear may contribute to wounds or compressed nerves. A 2023 systematic review of shoulder- and back-support devices also found reports of discomfort and effects involving muscle activity and neurovascular supply; incorrect fit and reduced freedom of movement were often identified as contributors.

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Movement, balance and task performance

Restricted mobility can make it harder to avoid a collision, recover balance or move quickly. NIOSH’s construction discussion notes concerns about balance recovery, distraction or reduced vigilance, and extra effort when a device resists movement outside its intended range. These issues deserve particular attention around moving equipment, at heights and in confined spaces. A device that is helpful for one movement or task is not thereby established as safe for another.

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Powered-device hazards and shared use

NIOSH identifies battery leakage or sudden discharge as possible sources of chemical or thermal burns. Follow the specific manufacturer’s instructions for batteries, charging, electrical safety, heat and maintenance. Shared devices also require attention to hygiene and cleaning. Over-reliance on an exoskeleton can be a concern if it leads people to overlook remaining hazards or other controls.

What does the evidence say about safety?

Evidence varies by device and task, and much of the available assessment is short-term or laboratory-based. In a 2023 systematic review, authors examined 36 studies of shoulder- and back-support devices: four were in-field studies and 32 were laboratory studies. Thirty studies reported discomfort and 16 reported limited usability. Those are counts of studies reporting effects, not the share of users affected. The review also described reported effects involving mobility, balance, posture, gait, precision and task performance. Active exoskeletons were understudied, and short-term findings cannot establish long-term safety in varied workplaces.

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NIOSH’s 2017 construction discussion likewise says evidence is insufficient to determine complete long-term safety profiles. Laboratory findings may not predict what happens across different users, devices, work rates and environments. The sources do not establish which specific model is safest for an individual or workplace.

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How do workplace exoskeletons differ from medical devices?

“Exoskeleton” covers different devices and uses. In the United States, a powered lower-extremity exoskeleton intended for medical use by a person with paralyzed or weakened lower limbs is a prescription Class II medical device. That regulatory status does not automatically apply to passive workplace back or shoulder supports.

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Powered lower-extremity medical exoskeleton, United States Prescription Class II device for medical use on paralyzed or weakened lower limbs. Under 21 CFR 890.3480, special controls include biocompatibility; electromagnetic, electrical, thermal and mechanical safety; battery safety; software hazard analysis; simulated-use and durability testing; clinical testing; training; and user warnings and maintenance information.
Workplace exoskeleton, such as a passive back or shoulder support Do not assume the medical-device classification or requirements apply. NIOSH frames workplace use as something to evaluate within broader ergonomics and safety work, including the task, wearer, fit, environment, benefits and residual hazards.

The FDA classification database lists recognized standards for powered exoskeletons, including IEC 80601-2-78 for medical robots used in rehabilitation and related movement functions. For the covered US medical-device class, the regulation requires a training program for the clinician, user and companion, as well as user warnings and maintenance information. These requirements are specific to that regulated category; they should not be generalized to every workplace device.

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How can users and employers reduce risk?

Evaluate the exoskeleton as one part of a safety program, not as a substitute for hazard controls or an overall ergonomics process. NIOSH recommends matching the device to the task and addressing any risks that remain.

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  1. Define the use. Identify the exact task, body region the device is meant to support, wearer and work environment. Do not assume a benefit or safe result transfers from one task to another.
  2. Check fit and movement. Follow device-specific fitting instructions. Check for discomfort, pressure points and restricted movement. Stop and follow the manufacturer’s instructions if problems arise, including signs that could indicate compressed nerves.
  3. Assess movement and load. Consider whether the wearer can balance, recover from a stumble, avoid collisions, move freely and reach controls. Check whether the device may shift load to the back, legs or another body region.
  4. Review the hazards around the task. Consider moving equipment, work at heights, confined spaces and any situation requiring a fast response. Account for possible distraction or resistance to movements outside the device’s intended range.
  5. Train users and supervisors. Make sure users understand the device’s intended use, safeguards, limitations and safe operating environments. For regulated US powered lower-extremity medical exoskeletons, follow the required training program and warnings.
  6. Maintain powered devices and manage shared use. Follow the manufacturer’s battery, charging, electrical, thermal and maintenance instructions. Establish appropriate hygiene and cleaning practices for devices used by more than one person.
  7. Keep other controls in place. Evaluate residual risk and retain appropriate hazard controls and ergonomic measures rather than relying on the exoskeleton alone.

What should healthcare settings consider?

Exoskeleton use for patient handling is an emerging area, not an established universal replacement for Safe Patient Handling and Mobility programs. NIOSH recommends evaluating it alongside those existing programs. A healthcare assessment should consider patient comfort and safety, the wearer’s ability to respond quickly, disinfection, restricted spaces and compatibility with other medical devices.

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The occupational need is substantial but does not prove a device works. NIOSH reported that hospital workers had nearly twice the all-industry average rate of overexertion injuries, based on Bureau of Labor Statistics data cited in its 2017 discussion. NIOSH also reported 18,090 musculoskeletal disorder cases among nursing assistants in 2017, with more than half involving back injuries. These figures describe background injury burden, not the effectiveness or safety of exoskeletons.

When is an exoskeleton a poor fit?

A device may be unsuitable when its fit, restrictions or added bulk interfere with safe movement or with the task’s demands. A decision should be based on the exact device and environment, not on the general promise that exoskeletons reduce effort. A qualified professional assessment and the manufacturer’s instructions are necessary for device- and user-specific decisions; the available evidence does not provide individual medical clearance or identify a universally safest model.

Product prices and availability are accurate as of the date/time indicated and are subject to change. Any price and availability information displayed on Amazon at the time of purchase will apply.

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