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CAD/CAM Ti-bases for CEREC® and inLab®

IPD Ti-bases compatible with Sirona® CEREC®

A digital solution for implant-supported crowns connecting a compatible CEREC® library, block geometry, precisely optimised Ti-base and a TiN-coated screw.

Titanium Grade VFull-surface TiN coatingGingival heights by platform
IPD Ti-base compatible with Sirona CEREC with TiN surface
Spiral groovesmechanical retention for cementation
0,5 / 1,5 / 2,5 mmtypical gingival heights
CEREC® + inLab®library and block geometry
Class IIb medical deviceClassification stated in the IPD product presentation.
Titanium Grade VA rigid, precisely machined base for the hybrid crown.
TiN surfaceGolden shade, aesthetics and surface properties.
Broad compatibilityLibrary, block and platform within one conversion system.
Digital workflow

From scan to intraoral fixation of the hybrid crown

The IPD presentation describes five sequential steps: digital acquisition, CAD design, manufacture of the ceramic restoration, finishing and extraoral cementation onto the Ti-base, followed by intraoral fixation.

1

Digital scan

The original scan body and correctly selected library transfer the implant position into the CAD environment.

2

CAD design

In CEREC® or inLab®, the correct library geometry is assigned and the implant crown is designed.

3

Manufacturing

The ceramic block is milled to the designed shape. The material and block must match the selected library.

4

Finishing and cementation

After sintering or crystallisation and glazing, the restoration is cemented extraorally onto the Ti-base.

5

Intraoral fixation

The completed hybrid crown is secured to the implant using the torque specified for the system.

Diagram of crown, fixation screw and implant Ti-base
Hybrid-crown principle: ceramic restoration, fixation screw and compatible Ti-base.
Control points
The same platform throughout the chainThe Ti-base, fixation screw, library, block geometry and implant platform must form a matching combination.
Correct gingival heightHeight is selected according to the mucosal profile, prosthetic space and the options available for the specific connection.
Torque according to the systemThe table below shows recommended torques from the 2024 Conversion Guide; verify the current instructions for use before clinical use.
Details make the difference

Retention, anti-rotation and geometry optimised for CEREC®

IPD states that the geometry and parameters are optimised for the original workflow. The design combines spiral grooves for mechanical retention of the cemented restoration, locking geometry for scan-body orientation and anti-rotation, and multiple gingival heights depending on the implant connection.

Spiral grooves

They increase the functional surface area and improve mechanical anchorage of the cemented ceramic restoration.

Locking anti-rotational profile

Helps provide unambiguous orientation of the scan body and implant-supported crown.

Multiple gingival heights

For most ranges 0.5 / 1.5 / 2.5 mm; for selected connections 0.8 mm or 1 / 2 / 3 mm.

Detail of spiral grooves and anti-rotational geometry of the IPD CEREC Ti-base
Detail of the crown section: spiral retention and mechanical locking geometry for the digital workflow.
Conversion Guide 2024

Implant platform, reference, screw, torque, library and block

The complete conversion table is reproduced directly in HTML. It can be searched by manufacturer, platform, IPD reference or CEREC® library.

RangeImplant systemImplant platformØ prosthetic baseGingival heightsTi-base referencesTiN screwTorqueCEREC® libraryBlok
AANobel Biocare® Brånemark System®Ø3.5Ø4.40.5 / 1.5 / 2.5IPD/AA-IN-00/SI · 02/SI · 04/SIIPD/AA-TN-00/TIN35 NcmNB B 3.4L
AANobel Biocare® Brånemark System®Ø4.1Ø5.00.5 / 1.5 / 2.5IPD/AA-IR-00/SI · 02/SI · 04/SIIPD/AA-TR-00/TIN35 NcmNB B 4.1L
ADNobel Biocare® Nobel Active® / Replace® ConicalNP Ø3.5Ø3.850.5 / 1.5 / 2.5IPD/AD-IN-00/SI · 02/SI · 04/SIIPD/AA-TN-00/TIN35 NcmB C 3.4S
ADNobel Biocare® Nobel Active® / Replace® ConicalRP Ø4.3Ø5.00.5 / 1.5 / 2.5IPD/AD-IR-00/SI · 02/SI · 04/SIIPD/AA-TR-00/TIN35 NcmNB B 4.1L
BBBiomet 3i® Certain®NP Ø3.4Ø3.850.5 / 1.5IPD/BB-IN-00/SI · 02/SIIPD/BB-TR-01/TIN20 NcmB C 3.4S
BBBiomet 3i® Certain®RP Ø4.1Ø4.650.5 / 1.5IPD/BB-IR-00/SI · 02/SIIPD/BB-TR-01/TIN20 NcmB C 4.1L
DAStraumann® Tissue Level®RN Ø4.8Ø5.00.8IPD/DA-IR-00/SIIPD/DA-TR-01/TIN35 NcmS SO 4.8L
DBStraumann® Bone Level®NC Ø3.3Ø4.451 / 2 / 3IPD/DB-IN-00/SI · 02/SI · 04/SIIPD/DB-TR-00/TIN35 NcmS BL 3.3L
DBStraumann® Bone Level®RC Ø4.1Ø4.551 / 2 / 3IPD/DB-IR-00/SI · 02/SI · 04/SIIPD/DB-TR-00/TIN35 NcmS BL 4.1L
EAAstra® Osseospeed TX™Ø3.5–Ø4.0Ø4.251 / 2 / 3IPD/EA-IR-00/SI · 02/SI · 04/SIIPD/EA-TR-02/TIN20 NcmFX 3.8S
EBAstra® Evolution®S Ø3.6Ø3.850.5 / 1.5 / 2.5IPD/EB-IN-00/SI · 02/SI · 04/SIIPD/EB-TN-00/TIN20 NcmB C 3.4S
EBAstra® Evolution®M Ø4.2Ø4.650.5 / 1.5 / 2.5IPD/EB-IR-00/SI · 02/SI · 04/SIIPD/EB-TR-00/TIN20 NcmB C 4.1L
FAZimmer® Screw Vent®Ø3.5Ø3.850.5 / 1.5 / 2.5IPD/FA-IN-00/SI · 02/SI · 04/SIIPD/FA-TR-00/TIN30 NcmB C 3.4S
FAZimmer® Screw Vent®Ø4.5Ø5.00.5 / 1.5 / 2.5IPD/FA-IR-00/SI · 02/SI · 04/SIIPD/FA-TR-00/TIN30 NcmNB B 4.1L
LBBioHorizons® Tapered InternalØ3.0Ø3.850.5 / 1.5 / 2.5IPD/LB-IT-00/SI · 02/SI · 04/SIIPD/LB-TR-01/TIN35 NcmB C 3.4S
LBBioHorizons® Tapered InternalØ3.5Ø3.850.5 / 1.5 / 2.5IPD/LB-IN-00/SI · 02/SI · 04/SIIPD/LB-TR-01/TIN35 NcmB C 3.4S
LBBioHorizons® Tapered InternalØ4.5Ø5.00.5 / 1.5 / 2.5IPD/LB-IR-00/SI · 02/SI · 04/SIIPD/LB-TR-00/TIN35 NcmNB B 4.1L
TBMIS® C1 / V3®StandardØ5.110.5 / 1.5 / 2.5IPD/TB-IR-00/SI · 02/SI · 04/SIIPD/TB-TR-00/TIN30 NcmNB B 4.1L

Source: IPD CEREC® Ti-Base Conversion Guide 2024 and IPD product materials. For the Biomet 3i® Certain® range, the HTML references are standardised by platform as BB-IN for NP and BB-IR for RP. Always verify current availability, recommended torque and final compatibility in the valid instructions for use or with technical support.

Indicative height selection

Gingival height according to the soft-tissue profile

The Conversion Guide provides an indicative relationship between the patient’s gingival height and the recommended Ti-base height. It is a guide, not a substitute for clinical assessment, material space or the rules of the specific implant system.

< 1,0 mmrecommended GH 0.5
1,0 mmGH 0.5 or GH 1
2,0 mmGH 1 or GH 1.5
3,0 mmGH 2 or GH 2.5
≥ 4,0 mmGH 2.5 or GH 3
Two IPD Ti-bases compatible with CEREC in different geometries
Different implant platforms require the corresponding geometry, gingival height, library and block.
TiN surface and professional context

Golden surface: aesthetics, biocompatibility and limits of the evidence

The IPD presentation emphasises the aesthetic benefit of TiN and antibacterial surface properties. Below, we distinguish between what laboratory studies show and what cannot automatically be extrapolated to the specific clinical product.

Brunello et al., 2018

An in-vitro comparison of untreated Ti6Al4V, anodised surfaces, TiN and ZrN confirmed compatibility with gingival fibroblasts. ZrN showed the highest antibacterial activity; TiN also inactivated biofilm, but less markedly.

PLOS ONE · DOI

Zhurakivska et al., 2020

A laboratory study reported greater gingival-fibroblast proliferation and lower Streptococcus gordonii growth on nitrided and anodised titanium than on untreated titanium.

Prosthesis · DOI

Del Castillo, 2022

A review summarises the technical and clinical context of TiN coatings on implant abutments, including aesthetics and a possible reduction in early bacterial colonisation.

PubMed

Important: The cited studies are not direct clinical trials of the specific IPD CEREC® Ti-base. Some results are in vitro, and Brunello et al. also compares TiN with ZrN. The website therefore does not attribute a therapeutic effect to the product and uses a factual description of the surface and available laboratory evidence.

Frequently asked questions

What to verify before designing and ordering

The key is to maintain consistency between the implant platform, Ti-base, screw, gingival height, library and block geometry.

How is the Ti-base integrated into the CEREC® workflow?

After digital scanning, the corresponding library and block are selected in the CAD environment, the crown is designed and milled, the ceramic is finished, the restoration is cemented extraorally onto the Ti-base and the completed crown is fixed intraorally.

Is special preparation required?

No special clinical preparation of the product is stated in the presentation. However, knowledge of the CAD/CAM workflow, correct scanning equipment, a compatible library and a validated cementation protocol are essential.

What restorations can be made?

According to the supplied presentation, the range is intended for implant-supported single crowns. Non-engaging variants were described as under development at the time of the source material; current status must be verified.

How do I verify correct compatibility?

Find the manufacturer and implant platform in the conversion table, then check the IPD reference, screw, torque, CEREC® library and block size. Similar component shape is not sufficient evidence of compatibility.

Why are spiral grooves important?

The grooves increase the retentive geometry of the coronal part of the Ti-base and support mechanical anchorage of the cemented ceramic restoration.

Need to verify the CEREC® library, block and specific reference?

Send us the implant brand, system, platform and planned gingival height. We will verify the matching Ti-base, fixation screw, torque and library geometry.

CEREC®, inLab® and Sirona® are trademarks of their respective owners. They are mentioned solely to identify compatibility. IPD and Exklusiv Dent s.r.o. do not own these trademarks. Use the product according to the current instructions for use and validated working procedures.

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