Distribution & training
Surgeons, prosthetists, distributors
Onboarding for certified OPL centres, distribution enquiries, and surgeon training requests across all jurisdictions where OPL is approved.
Email the partnerships team Contact
Tell us about your clinic, your patients, or your question.
OI is the legal manufacturer of the OPL system. We work with surgeons, prosthetists, distribution partners, regulators, and auditors. Patient enquiries are handled by our clinical sibling organisations — details below.
Who to talk to
Routes for the most common enquiries.
Regulatory & documents
IFUs, audit packs, and compliance
IFU and surgical technique guide access, jurisdiction-specific compliance questions, and audit support for notified bodies and competent authorities.
Email regulatory affairs Clinical care
Patient enquiries
OI does not provide direct patient care. Our clinical sibling organisations manage patient enquiries, assessments, and surgical pathways.
Visit Osseointegration Group Adverse events
Report a device-related adverse event.
Clinicians and patients can report any device-related adverse event to our regulatory team. We triage within one business day and report onward to competent authorities under the timelines required by each jurisdiction.
For life-threatening or serious public-health events, also contact your local competent authority directly (TGA, MHRA, BfArM, etc.).
General enquiry form
Prefer a form?
Submit your enquiry below and we’ll route it to the right team. We respond within one business day.
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The general enquiry form will be embedded here at launch. In the meantime, please email hello@osseointernational.com.
Legal entity
Osseointegration International Pty Ltd
- hello@osseointernational.com
- ABN
- 15 604 356 676
- Registered office
- Sydney, New South Wales, Australia
- Role
- Legal manufacturer of the OPL osseointegrated prosthetic system
Build a better standard of care