Screw Retained Crown & Bridge
Screw-retained crowns and bridges provide direct implant access and retrievability while supporting controlled emergence, functional contacts and case-appropriate CoCr or titanium framework design.
Screw-retained implant prosthesis solutions are designed for easy retrievability, strength and predictable implant-supported restoration outcomes.
From single-unit crowns to full-arch rehabilitation, the workflow considers implant components, restorative space, framework design, emergence and functional occlusion.

Screw-retained crowns and bridges provide direct implant access and retrievability while supporting controlled emergence, functional contacts and case-appropriate CoCr or titanium framework design.
All On X provides a flexible full-arch pathway based on the planned number and distribution of implants, enabling a case-specific prosthetic design for complex rehabilitation.
Answers about planning, records, components, production and delivery.
Screw-retained implant prosthesis solutions are designed for easy retrievability, strength and predictable implant-supported restoration outcomes.
Suitability depends on implant position, restorative space, occlusion, tissue conditions, framework requirements and the treatment plan approved by the clinician.
Send the prescription, implant-level or abutment-level scan or impression, opposing arch, bite record, implant system details, shade and relevant clinical photographs.
The manufacturer, platform, connection, component type and scan body information help the laboratory select compatible components and design the restoration correctly.
The team reviews the records, implant positions, restorative space, emergence, occlusion and material requirements before CAD design and manufacturing.
Laboratory quality checks review the prescribed components, framework or restoration fit, contacts, occlusion, design and finishing before dispatch.
Yes. Early communication and complete diagnostic records help the laboratory review multi-implant and full-arch requirements before production begins.
Turnaround depends on case complexity, components, materials and approvals. The schedule is confirmed after the submitted records and prescription are reviewed.
Send the prescription, implant system details, scan or impression and supporting records for laboratory review.
Send an implant case