Stock Abutment + MLS Crown
A compatible stock abutment paired with an MLS crown offers a practical cement-retained workflow for suitable implant positions and restorative requirements.
Cement-retained implant prostheses are designed for implant-supported crowns and bridges where the final restoration is fixed using dental cement.
Stock abutment, Ti-Base and zirconia-abutment pathways allow the restorative plan to balance component compatibility, emergence profile, aesthetics, occlusion and clinical cementation.

A compatible stock abutment paired with an MLS crown offers a practical cement-retained workflow for suitable implant positions and restorative requirements.
This option combines a stock implant abutment with a zirconia crown for strength, controlled contours and improved tooth-coloured aesthetics.
A Ti-Base provides a manufactured titanium connection while the cemented MLS crown is designed for the required emergence, occlusion and restorative form.
The Ti-Base and zirconia crown combination supports a precise implant connection with a strong, aesthetic cement-retained suprastructure.
A zirconia abutment supported by a Ti-Base and restored with a zirconia crown allows greater control of emergence and colour in aesthetic implant locations.
MLS and zirconia pontics are shaped within implant-supported bridge designs to support cleansable contours, appropriate tissue relationships and consistent restorative aesthetics.
Answers about planning, records, components, production and delivery.
Cement-retained implant prostheses are designed for implant-supported crowns and bridges where the final restoration is fixed using dental cement.
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