Vigilance & Adverse Event Reporting

Report a serious incident or adverse event related to an Osteoneks medical device.

Reporting an Adverse Event

If you suspect that a serious incident or adverse event has occurred in connection with an Osteoneks medical device, you are required to report it to the relevant national competent authority (e.g., MHRA in the UK) and to Osteoneks.

Contact for Vigilance Reports

To submit a vigilance report to Osteoneks, contact our regulatory affairs team at: Unit FF 13, Al-Hikmah Centre, 28 Track Road, Batley, WF12 7AA | Tel: (+44) 07405891046