LATEST NEWS
All Items
Latest news

VIEW POST
Lojer expands its product range with surgery room solutions and medical lights.

VIEW POST
We are going to have an interesting and enlightening discussion and demonstration with osteopath Kevin Collet how Manuthera 242 differs from a traditional treatment table, and what...

VIEW POST
The Institute of Education in Orthopaedic Osteopathy (OOKK) in Helsinki uses Lojer's Manuthera 242 examination and treatment tables for teaching purposes. The table has been very p...

VIEW POST
The exhibition will be held from 24th of January until 27th of January at The Dubai World Trade Centre. You will find us at the heart of the exhibition area, Hall 3 Stand B30.

VIEW POST
In November, all three of Lojer's factories in Finland were granted environmental certification for their environmental management systems in accordance with the international ISO...

VIEW POST
In the final article of the "Lojer Speed Pulleys" blog series you can find versatile tips on how to utilize the Speed Pulley for different parts of the body.

VIEW POST
With the Lojer Speed Pulley the resistance stays the same throughout the exercise, where as with f.ex. rubber bands the last part of the movement is always the toughest one and it...

VIEW POST
Dr. Hassan has treated thousands of patients with the Manuthera Treatment Table - and now he is sharing his best techniques, approaches and methods for free!

VIEW POST
Lower limb injuries can vary from mild to severe injuries that require surcigal operation. The injured part can be joint, bone, muscle, tendon or the patient may experience non-spe...

VIEW POST
Movement Fysios needed a movable pulley since they use it in different locations inside the clinic depending on the customer's needs and other equipment needed for the rehabilitati...

VIEW POST
The new catalogue is ready. In the catalogue you will find all our Medical Wellness products as well as updated and more detailed product information.

VIEW POST
The application of the MDR (EU 2017/745) has started on 26 May 2021 after a four-year transition period. All Class I healthcare devices must comply with the new regulation.