Secure, browser-based 3D planning and auditable manufacturing handoff for hospitals and clinical teams.
Reduce case preparation time, meet documentation requirements for regulatory audits, and integrate with existing hospital IT infrastructure without disruptive change management.
Review and approve patient-specific guides in a browser — no installed software, no file-sharing workarounds. Every annotation and approval is attributed and permanently recorded.
Receive production-ready packages with complete provenance: who approved, when, what version, and what QC checks were performed. Fewer intake failures, faster production starts.
Traditional planning takes 2–3 weeks, relies on manual CAD work, and fragments communication across insecure channels.
100% browser-based platform.
No installs required.
FDA-Cleared Quality Workflows: Ovynor strictly adheres to standards required for patient-specific implants (PSI) and anatomical models. Our infrastructure guarantees ISO 13485 compliance through every stage of the design lock.
DICOM to 3D Printing: We provide a robust bridge connecting pre-operative Virtual Surgical Planning (VSP) software directly to point-of-care 3D printing labs, preserving high-fidelity anatomical data from AI segmentation to final production.
Secure Surgical Case Management: Reduce clinical risk with an end-to-end encrypted orchestrator. Every interaction from the operating room down to the lab is tracked, bringing a verifiable digital thread that protects clinical data.
Security and compliance are not afterthoughts; they are the foundational layers of the Ovynor architecture.
We are currently onboarding a select group of hospitals, surgeons, and manufacturing labs through closed pilot programs.