Action Reliever
Action Reliever
Action Reliever
Action Reliever
Action Reliever
Action Reliever
Action Reliever

Action Reliever

Action Reliever

OA knee brace

Clinically proven



Adjustable 3-point leverage system with inelastic straps to provide alignment support and off-loading of the affected compartment.

An anatomically-shaped knitting for even compression.

The brace is maintained on the leg thanks to the silicone-coated threads at the top of the knee brace.

Easy to use thanks to the magnetics fasteners.



  • Verify the product’s integrity before every use.
  • Do not use the device if it is damaged.
  • Choose the appropriate size to fit the patient, referring to the size chart.
  • If the measurements taken do not correspond to the same size, favor the size corresponding to measurement A.
  • It is recommended that a healthcare professional supervises the first application.
  • Strictly comply with your healthcare professional’s prescription and recommendations for use.
  • This product is intended for the treatment of a given condition. Its duration of use is limited to this treatment only.
  • For hygiene and performance reasons, do not re-use the product for another patient.(
  • It is recommended to adequately tighten the device to achieve support/immobilisation without restricting blood circulation
  • In the event of discomfort, significant hindrance, pain, variation in limb volume, abnormal sensations or change in colour of the extremities, remove the device and consult a healthcare professional
  • In the event of any modification in the product's performance, remove it and consult a healthcare professional.
  • Before any sports activity, check the compatibility of the use of this medical device with your healthcare professional.
  • This device has magnetic components.
  • Do not wear the product in a medical imaging device.
  • Do not use the device in case of application of certain products on the skin (creams, ointments, oils, gels, patches...).

  • This device can cause skin reactions (redness, itching, burns, blisters...) or wounds of various degrees of severity.

  • Any serious incidents occurring related to the device should be reported to the manufacturer and to the competent authority of the Member State in which the user and/or patient is resident.


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