Catalogue - Phibo® · catalogue may cause serious patient health problems as well as total loss of...

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Transcript of Catalogue - Phibo® · catalogue may cause serious patient health problems as well as total loss of...

Page 1: Catalogue - Phibo® · catalogue may cause serious patient health problems as well as total loss of the product warranty. The DEFCON Tissue Care implant system has been designed for
Page 2: Catalogue - Phibo® · catalogue may cause serious patient health problems as well as total loss of the product warranty. The DEFCON Tissue Care implant system has been designed for

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2IMPORTANT BEFORE USE

DEFCON Tissue Care®

In its innovative and patented design, the

DEFCON Tissue Care® implant system

incorporates advanced technological features

developed only for professionals who

understand technology as an advantage, and

design as a benefit.

DEFCON Tissue Care® complies with

all the demands and requirements of

European Directive 93/42/EEC regarding the

manufacture and distribution of medical-

sanitary products. The products of the

DEFCON Tissue Care® implant system have

CE marking, evaluated by NB 0123. The

Quality System of Impladent, S.L. complies

with the strictest international quality norms,

and is certified according to ISO 9001 and

ISO 13485 by TÜV SÜD Product Service,

guaranteeing perfect product quality, and

assuming as its sole objective a constant

increase in client satisfaction.

The use of the other components or products

not original of DEFCON Tissue Care®, and

which come into contact with the originals of

the implant system according to the original

design specifications, may cause serious

patient health problems, since they have

not been contemplated for use with those

elements referenced in the documentation

supplied by the manufacturer.

Any use of non-original components or

instruments in this procedure, that come into

contact with the referred original components,

will automatically cancel any type of warranty

covering the DEFCON Tissue Care® products.

The use and application of the DEFCON

Tissue Care® dental implant system are

beyond the control of the manufacturer,

and the user is responsible for any damage

that may result from the use of the product.

Impladent, S.L. declines all responsibility

for damage derived from its incorrect

manipulation or use.

The documentation of the DEFCON Tissue

Care® implant system is periodically updated

according to the state of scientific and

technological knowledge. Users of the

DEFCON Tissue Care® system should request

product information on a regular basis and

take part in the regularly established training

courses on the product and technique. The

use and placement of DEFCON Tissue Care®

implants in inappropriate sectors, and the

use of surgical instruments or prosthetic

components not contemplated in this

catalogue may cause serious patient health

problems as well as total loss of the product

warranty. The DEFCON Tissue Care® implant

system has been designed for single (unit) or

multiple dental restorations according to the

traditional clinical processes reflected in this

documentation. Excluded from the warranty

are cases involving insufficient bone for

implant placement, clinical risk cases such

as sinus lift procedures, fillings, advanced

surgical techniques, cases of severe or

non-apt disparallelism between implants, and

other cases.

The DEFCON Tissue Care® implant system is

internationally distributed in various countries

with different technical and healthcare

regulations and laws; accordingly, there may

be differences from one country to another

in terms of the contents of the procedure.

Consult the exclusive DEFCON Tissue Care®

distributor in your country and request the

documentation relating to the products and

their availability.

Impladent, S.L. reserves the right to modify

and develop the products reflected in this

catalogue, without prior warning.

All rights reserved. Printing or processing

the contents of this publication in any

format requires prior written permission from

DEFCON Tissue Care®.

DEFCON® Implants, DEFCON® Cess-CAM,

Tissue Care®, TSA® Advance, TSA®, TSH®,

BNT®, Avantblast®, ProUnic®, ProUnic Plus®.

Duplit®, Softissue, International DEFCON

Group®, DEFCON® Prostodontics, DEFCON®

Scientific, are commercial and/or registered

trademarks of Impladent, S.L. DEFCON Tissue

Care® implants are protected by international

patents. Other products and accessories are

protected by patents or are patent pending.

The illustrations in this document are not

made to scale.

0123

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3CONTENTS:

Design of the implant: macrodesign / microdesign Page 04-05

Versatile, easy and reliable prosthetic connection Page 06-07

A solution for each restoration Page 08-09

Science and technology to obtain

predictable results Page 10-11

General characteristics Page 12-13

Restorations Page 14-15

Aesthetics and immediate loading Page 16

Screwed restorations Page 17-18

Cemented restorations Page 19

Overdenture restorations Page 19-20

Impression copings Page 20

Planning abutments Page 21

Instruments Page 22-26

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Microthread

The design of the implant neck incorporates microthreads offering distribution of the forces in the implant insertion phase. The critical point of the interface between bone and implant is located in the marginal cortical bone, where the highest stress values are observed. The microthread reduces stress upon the bone crest at the time of implant insertion, offering the advantage of improved primary stability.The biomechanical stimulation produced by the micro taps of the TSA® Advance implant favours the preservation of marginal bone in the implant osteointegration phase.

Self-tapping profile

The body of the TSA® Advance implant is self-tapping, and the outer tap design offers the following main advantages:· Minimally invasive characteristics.· Directional tapping, to facilitate implant

insertion and shorten the surgical times.· Reduction of the increase in bone

temperature during implant insertion.· Biomechanical stimulation of the bone

tissue.· Maximum implant stability upon

insertion.

Emergence profile

The innovative TSA® Advance implant design incorporates the creation of an emergence profile of 0.7 mm for the care, conformation and maintenance of the soft tissues. It ensures tissue stability, providing an implant-gum interface based on the hemidesmosomal junction, with the advantage of improved aesthetic results.

Anodised platform

The platform of the TSA® Advance implant includes colour coding of the series corresponding to the system involved: green for the ø 3.7 mm platform (series 3), blue for the ø 4.7 mm platform (series 4) and magenta for the ø 6.0 mm platform (series 5), thus allowing immediate identification of the implant series, even in the most delicate situations.

Avantblast® Surface(Patented)

Avantblast® is the surface of the DEFCON Tissue Care® implant system.Continuing in the line of research on implant surface treatment based on chemical action, Avantblast® offers advances and optimisation of biological response, improving upon the results obtained with acid-etched

DESIGN OF THE IMPLANT:MACRODESIGN / MICRODESIGN

surfaces and posterior passivating. Avantblast® combines key factors to facilitate biological response: implant surface increase through optimised roughness and increased thickness of the titanium dioxide layer. The Avantblast® surface is manufactured in a controlled manner under dual chemical action, offering exclusive properties thanks to its notorious porosity. The result is a morphology very similar to that of cancellous bone that optimises the osteointegration process, implant anchoring to bone, and clinical success. The exclusive morphology of the Avantblast® increases the effective surface of the implant while multiplying the thickness of the superficial TiO2 layer. All these factors afford improved implant - bone binding, with increased retention force, lower release of metal ions into the environment, and greatly improved humectability.

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Selection of scientific references

Surface:Clinical and Radiographic Behaviour of 290 dental implants with a surface treated with hydroufluric acid and passivated with hydrofluoric and nitric acid: early loading results after 2 years. Med Oral Patol Oral Cir Bucal 2006; 11:E281-5.José María Martínez-González, Cristina Barona Dorado, Jorge Cano Sánchez, María Flórez Rodriguez, Miriam Cantero Al varez.Conclusions: The implant survival rate was 98.56%. Results after the prosthetic loading of 279 implants (survival rate 98.56%) attest that early loading may a must be applied, after a rigorous planning and case selection. Physico-chemical characterization of the surface of 9 dental implants with 3 different surface treatments. Med Oral Patol Oral Cir Bucal 2005; 10:58-65.Daniel Rodríguez Rius, F. Javier García Sabán.

Conclusions: Avantblast treatment as a consequence and increased osseointegration and bone formation in contact with the surface of the implants when compared with other surfaces.

Osteointegration:Early Loading of 642 Defcon Implants: 1-Year Follow-Up. Journal of Oral and Maxillofacial Surgery 2007; 65 (11), 2317-2320.Miguel Penarrocha PhD, DDS , Celia Carrillo DDS, Araceli Boronat DDS and Eva Martí DDS, PhD.Conclusions: The implant survival rate is 98.13%. Microthread:The implant neck: smooth or provided with retention elements. A biomechanical approach.Clin Oral Implants Res. 1999 Oct;10(5):394-405.

Hansson S. Dpt. Pol. Mat. Chalmers, University of Technology, Göteborg, Sweden.

Primary stability:Resonance frequency analysis after the placement of 133 dental implants. Med Oral Patol Oral Cir Bucal 2006 May 1; 11(3):E272-6.Boronat,A., Peñarrocha,M., Martinez-Cortissoz,O., and Minguez-Martinez,I.Conclusions: The stability quotient of the implants on the day of surgery was 62.1, with an insertion force of 35.7 N.

For further information www.defconimplants.com

Microthread

Avantblast®

Anodised platform

Emergence profile

Self-tapping profile

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A VERSATILE, EASY AND RELIABLE PROSTHETIC CONNECTION

ProUnic® Advance abutment

New ProUnic® Advance abutment, witha single screw for screwed estorations.

The new ProUnic® Advance abutment incorporates a single screw for single and multiple screwed restorations.

It presents angulations in the upper cone to overcome disparallelisms of up to 30º between implants.

The new ProUnic® Advance abutmentconnects:· Internal hexagon of the implant. Affords hexed characteristic.· External hexagon of the implant. Affords hexed and fitting characteristics.· Internal cone of the implant. Affords stress distribution characteristics.· External cone of the abutment. Affords fitting with the definitive prosthesis.

Stress distribution

The global TSA® Advance and ProUnic® Advance abutment complex has been designed for improved stress distribution, offering the following advantages:· Greater stability.· Improved load distribution.· Increased durability of the implant and prosthesis.· Improved quality of life for patients.

Soft tissue care

The new ProUnic® Advance abutmentaffords force distribution along the long axis of the implant, stimulating soft tissue adhesion to the crown portion of the implant, and reducing stress at the implant-abutment connecting interface.

Colour code

The ProUnic® Advance abutments and their accessories include colour coding of the series corresponding to the system involved: green for series 3, blue for series 4 and magenta for series 5.

External hexagon

Internal cone

External cone

Internal hexagon

4 connections

The TSA® Advance implant has four connections: external hexagon, internal hexagon, external cone, internal cone. The hexagon connections afford antirotation of the prosthetic elements fixed to the implant in the two equidistant spatial planes.The connections of the internal cone and external cone direct the forces in the axial, radial and flexion directions, fixing the prosthesis to the implant.

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Single screw

ProUnic® Advance abutment

· Soft tissue care.· Angulations of the upper cone to overcome disparallelisms of up to 30º between implants.· Colour code.

Perfect binding:TSA® Advance implant and ProUnic® Advance abutment

· Greater stability.· Improved load distribution.· Increased durability of the implant and prosthesis.

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A SOLUTION FOR EACH RESTORATION

DEFCON® Cess-CAM offers reliable and precise products based on scientific - technical arguments that contribute to the best solutions in a competitive and differentiated manner, and over the long term. With a strong commitment to research and development, at the service of specialists in dental prostheses. DEFCON® Cess-CAM offers the latest advances in CAD-CAM technology. With a novel Technological Centre exclusively dedicated to the production of personalised prostheses, and with a robust quality system and total reliability in our products.

DEFCON® Cess-CAM offers the broadest range of materials made from Zirconium, Titanium, Cobalt Chrome and Plastics.

Zirconium

Titanium

Cobalt Chrome

This new business unit responds to the DEFCON® strategic plan. This plan aims to offer top level dental solutions in the field of implant systems, biomaterials and CAD-CAM, in order to satisfy the demand and present and future needs of clinics, prosthetic laboratories and patients.

DEFCON® Cess-CAM maintains the strong R&D dedication of the company, with the investment of important resources in this area. This synergy in the field of knowledge of implantology and prosthetic solutions based on CAD-CAM technology allows us to offer a broad catalogue of innovative and high-quality products, as well as a high added value technical support service.

DEFCON® Cess-CAM aims to facilitate access to CAD-CAM technology on the part of prosthetic laboratories, based on a robust technological package and personalised training courses programmed by experts in the field.

Personalised crowns

DEFCON® Cess-CAM, based on CAD-CAM technology, offers the possibility of producing personalised prostheses, ensuring highly aesthetic and precise results in an easy and safe manner, and improving clinical and laboratory processes.

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Improved aesthetics

The incorporation of aesthetic materials such as zirconium facilitates the manufacture of personalised prostheses with more predictable aesthetic results. The obtainment of passive fits superior to those afforded by the traditional method confers increased stability at the prosthesis-implant interface, caring for and maintaining the soft and hard tissues over the long term.

Greater passive fit

The DEFCON® Cess-CAM personalised prostheses system offers improved passive fit of the prosthesis, providing the clinician and laboratory with reliable and predictable long-term results.

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SCIENCE AND TECHNOLOGY TO OBTAINPREDICTABLE RESULTS

We are dedicated to science and technology

DEFCON Tissue Care® conducts studies in bioengineering, biocompatibility, experimental techniques and computer simulation on its products.

Our working philosophy is supported by our knowledge and is warranted by scientific studies. We contribute to improved patient quality of life, thanks to better oral health, greater comfort and aesthetics. DEFCON Tissue Care® continues to view comprehensive scientific research as the main reference of its values.

DEFCON Tissue Care® is carrying out a variety of multicentric clinical studies, continuing the success of its products in cooperation with the most reputable universities and national and international centres of reference.

Fatigue studies

To guarantee the reliability of the DEFCON Tissue Care®

products, we conduct fatigue studies according to the international ISO 14801 norm, with the following results:

With cyclic loading at a frequency of 15 Hz, applied to the global implant and abutment at an angle of 30º from its axis, we exceed 5 million cycles with forces in excess of 350 N.

DEFCON Tissue Care® , through its R&D+i activities, guarantees that the TSA® Advance implant design offers optimum mechanical and biological behaviour. The reports of reputed technological centres such as Applus or Inasmet, among others, certify this behaviour.

Studies of finite elements

The F.E.M. consists of rendering complex geometries discrete in smaller portions (finite elements), which can be studied by traditional solid mechanics. Mathematical relations of balance are established between these elements, from which a general result is obtained regarding the stresses and deformities of the studied structure.

Based on the computer simulations, the conclusions drawn are the following:

Mechanics: the geometric and balanced three-dimensional spatial design of its four connections allows stress distribution over the largest amount of surface - thus reducing the localised mechanical stress peaks. This prolongs material fatigue service life and approaches the requirements, objectives and functions of an ideal dental implant in the fixation and support of dental pieces.Biomechanics: the optimised design of the connections and their conical macrogeometrical characteristics ensure harmonic and coherent interaction of the implant with the biological supporting medium. The localised accumulation of stresses generated by the loads and chewing forces is avoided - thus allowing gradual energy release and force transmission to the bone-implant interface.

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11Selection of scientific references:

1. Buser, D. et al. Interface shear strength of titanium

implants with a sandblasted and acid-etched surface:

a biomechanical study in the maxilla of miniature pigs.

J Biomed Mater Res 45, 75-83 (1999).

2. Chee, W. et al. JOMI Current Issues Forum: Cemented

vs. Screw-retained implant prostheses: Which is better?

Int J Oral Maxillofac Implants 14, 137-141 (1999).

3. Hansson, S., & Norton, M. The relation between surface

roughness and interfacial shear strength for

Çbone-anchored implants. A mathematical model.

J Biomech 32, 829-836 (1999).

4. Martínez-González, J.M., Cano, J., Campo, J.,

Martínez, J.M.S., and García, F.J. Diseño de los implantes

dentales: estado actual.

Avances en Perodoncia 14, 129-136 (2002).

5. Masuda, T., Yliheikkila, P.K., Felton, D.A. & Cooper, L.F.

Generalizations regarding the process and phenomenon

of osseointegration. Part I. In vivo studies.

Int J Oral Maxillofac Implants 13, 17-29 (1998).

6. Misch, C.E., Bidez, M.W. & Sharawy, M. A bioengineered

implant for a predetermined bone cellular response to

loading forces. A literature review and case report.

J Periodontol 72, 1276-1286 (2001).

7. Nishiguchi, S. et al. The effect of heat treatment on

bone-bonding ability of alkali-treated titanium.

Biomaterials 20, 491-500 (1999).

8. Polmear IJ, (1981). “Light alloys. Metallurgy of the light

metals”. Metallurgy and materials Science Series.

Arnold. London. Pp. 239-278.

9. Semlitsch MF, Panic B, Weber H and Schoen R.(1981).

“Comparison of the fatigue strength of femoral prosthesis

stems made of forged Ti-Al-V and Cobalt base alloys”.

In titanium Alloys in Surgical Implants. Luckey and

Kubli Eds.

ASTM STP 796. Philadelphia pp.120-135.

10. Simmons,C.A., Meguid,S.A. & Pilliar,R.M. Differences

in osseointegration rate due to implant surface geometry

can be explained by local tissue strains.

Journal of Orthopaedic Research 19, 187-194 (2001).

11. Wong,M., Eulenberger,J., Schenk,R. & Hunziker,E.

Effect of surface topology on the osseointegration of

implant materials in trabecular bone.

J Biomed Mater Res 29, 1567-1575 (1995).

12. Zienkiewicz, O.C. The finite elements method (4th edition).

McGraw-Hill, ISBN 84-481-0178-2.

Finite element simulation techniques.

Test machine (high frequency).

Mechanical testing of fatigue life. Test machine (high frequency).

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Insertion height

The TSA® Advance implant has been designed to position the implant shoulder 0.7 mm above the bone crest, leaving this length of smooth neck as biological space for adhesion and sealing of the binding epithelium. The drilling length for implant insertion is the length of the implant minus 0.7 mm.

All TSA® Advance implants are made of grade II titanium from titanium bars obtained by cold instrumentation according to the ASTM-F67 norm.

Note: the TSA® Advance S5 Short implants cannot be inserted in single (unit) cases. Splinting is always required to improve distribution of the chewing loads. They cannot be used in immediate loading – two step surgery being required for restoration.

1Avantblast® treatment to 0.7 mm of the shoulder. 2Cover screw included. Colour anodised according to series.3The healing abutments have no colour code. Titanium.

GENERAL CHARACTERISTICS

Reference Length TSADV 03.085 8.5 mm

TSADV 03.100 10.0 mm

TSADV 03.115 11.5 mm

TSADV 03.130 13.0 mm

TSADV 03.145 14.5 mm

TSADV 03.160 16.0 mm

Healing abutment3 Reference Height010.3015 1.5 mm

010.3030 3.0 mm

010.3050 5.0 mm

010.3070 7.0 mm

Cover screw2

Advance S3

S3Body 3.6 mm

Microthreads2.5 mm

Internal thread 1.6

Anodised cone and hexagon in green

Machined neck0.7 mm1

Surfacetreated withAvantblast®

Implant length

Platform 3.7 mm

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Cover screw2 Cover screw2

Healing abutment3 Reference Height010.4015 1.5 mm

010.4030 3.0 mm

010.4050 5.0 mm

010.4070 7.0 mm

Healing abutment3 Reference Height010.5015 1.5 mm

010.5030 3.0 mm

010.5050 5.0 mm

Reference Length TSADV 04.085 8.5 mm

TSADV 04.100 10.0 mm

TSADV 04.115 11.5 mm

TSADV 04.130 13.0 mm

TSADV 04.145 14.5 mm

TSADV 04.160 16.0 mm

Reference Length TSADV 05.085 8.5 mm

TSADV 05.100 10.0 mm

TSADV 05.115 11.5 mm

TSADV 05.130 13.0 mm

Reference Length TSADV 05.060 6.0 mm

TSADV 05.070 7.0 mm

Advance S4

S5 S5 ShortS4

Advance S5 Advance S5 Short

Body 4.2 mm

Body 5.5 mm

Body 5.5 mm

Internal thread 1.8

Internal thread 1.8

Internal thread 1.8

Microthreads2.5 mm

Microthreads2.5 mm

Microthreads1.6 mm

Anodised cone and hexagon in blue

Anodised cone and hexagon in magenta

Anodised cone and hexagon in magenta

Implant length Implant lengthSurfacetreated withAvantblast®

Surfacetreated withAvantblast®

Surfacetreated withAvantblast®

Implant length

Machined neck0.7 mm1

Machined neck0.7 mm1

Machined neck0.7 mm1

Platform 4.7 mm

Platform 6.0 mm

Platform 6.0 mm

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RESTORATIONS

SINGLE

OVERDENTURESRetained bar

SCREWED

ProUnic® Advance

CEMENTED

MULTIPLE

CEMENTED

ProUnic® Advance ProUnic® abutment Aesthetic Non-hexed

SCREWED

ProUnic® Advance

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Retained ballLocator® DEFCON® Cess-CAM

ProUnic Plus® ProUnic® abutment Aesthetic Non-hexed

Drillable abutment Angled abutment

Angled abutmentDrillable abutment

Ball abutmentLocator® Titanium and Cobalt Chrome

ProUnic Plus® DEFCON® Cess-CAM Zirconium, Titanium and Cobalt Chrome

DEFCON® Cess-CAM Zirconium, Titanium and Cobalt Chrome

DEFCON® Cess-CAMTitanium and Cobalt Chrome

DEFCON® Cess-CAM Zirconium, Titanium and Cobalt Chrome

ProUnic® abutment Aesthetic Hexed

*Locator® is a registered trademark of Zest Anchors, Inc.

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ProUnic Plus®

Series Reference Designation

S3 167.3000 ProUnic®Plus.

S4 167.4000 Titanium.

S5 167.5000

S3 013.3000 ProUnic Plus®abutment.

S4 013.4000 Titanium.

S5 013.5000

S3 014.3010 ProUnic Plus®abutment. Titanium.

S4 014.4010 Transgingival 1 mm.

S5 014.5010

S3 014.3020 Transgingival 2 mm.

S4 014.4020

S3 014.3030 Transgingival 3 mm.

S4 014.4030

S3 018.3000 Laboratory screw.

S4 018.4000 Titanium.

S5 018.5000

S3 019.3000 Final clinical screw.

S4 019.4000 Titanium.

S5 019.5000

S3 060.3000 Coif for ProUnic Plus®provisional restorations.

S4 060.4000 Plastic.

S5 060.5000

S3 099.3000 ProUnic Plus® protective cap.

S4 099.4000 Plastic.

S5 099.5000

S3 062.3000 ProUnic Plus® impression transfer.

S4 062.4000 Plastic.

S5 062.5000

S3 061.3000 ProUnic Plus® analog.

S4 061.4000 Titanium.

S5 061.5000

Important: use specific instrumentation 1.25 mm, torque 35 Ncm.

All series of the ProUnic® Advance and ProUnic® product range have their colour code according to the series involved.

The DEFCON® implant system has been designed to simplify and reduce the clinical processes and restoration times, yielding improved aesthetic results and patient comfort from the start, and with the aim of ensuring tissue care and maintenance.

AESTHETICS AND IMMEDIATE LOADINGProvisional restorations with ProUnic® Plus

Immediate aesthetics: easy and simple

1 2 43 1. Placement of the ProUnic Plus® abutment over the implant.2. Placement of the provisional coping.3. Placement of the provisional crown.4. Placement of the final clinical screw.

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ProUnic® Advance

Series Reference Designation

S3 052.3001 ProUnic® Advance abutment. S4 052.4001 Includes clinical screw.S5 052.5001 Titanium.

S3 052.3110 ProUnic® Advance abutment. S4 052.4110 Includes clinical screw.S5 052.5110 Titanium. Transgingival 1 mm.S3 052.3120 Transgingival 2 mm.S4 052.4120 S3 052.3130 Transgingival 3 mm.S4 052.4130

S3 055.3000 ProUnic® Advance clinical screw.S4 055.4000 Titanium.S5 055.5000

S3 055.3010 ProUnic® Advance clinical screw. Titanium.S4 055.4010 Transgingival 1 mm. S5 055.5010S3 055.3020 Transgingival 2 mm.S4 055.4020 S3 055.3030 Transgingival 3 mm.S4 055.4030

S3 053.3100 Hexed casting cylinder. S4 053.4100 Plastic. S5 053.5100

S3 053.3200 Non-hexed casting cylinder.S4 053.4200 Plastic.S5 053.5200

S3 063.3000 ProUnic® Advance laboratory screw.S4 063.4000 Titanium.S5 063.5000

S3 063.3010 ProUnic® Advance laboratory screw. Titanium.S4 063.4010 Transgingival 1 mm. S5 063.5010S3 063.3020 Transgingival 2 mm.S4 063.4020 S3 063.3030 Transgingival 3 mm.S4 063.4030

Important: use specific instrumentation 1.25 mm, torque 35 Ncm. All series of the ProUnic® Advance and ProUnic® product range have their colour code according to the series involved.

SCREWED RESTORATIONSProUnic® Advance abutment

Heights, degrees and angles ProUnic® Advance

· ProUnic® Advance abutment S3 · Height from implant platform: 2.13 mm · Abutment conicity: 15º · Maximum angle between implants: 30º

· ProUnic® Advance abutment S5 · Height from implant platform: 2.55 mm · Abutment conicity: 15º · Maximum angle between implants: 30º

2.67 mm

30º

15º 15º

S4

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Aesthetic ProUnic® Hexed

Series Reference Designation

S3 039.3000 Aesthetic ProUnic® abutment. Hexed.

S4 039.4000 Titanium.

S3 167.3010 Aesthetic ProUnic® Driver.

S4 167.4010 Titanium.

S3 041.3100 ProUnic® abutment hexed casting cylinder.

S4 041.4100 Aesthetic hexed for screwed

crowns. Plastic.

S3 040.3000 Titanium laboratory screw

S4 040.4000 Aesthetic ProUnic® abutment. Hexed.

S3 045.3000 Final titanium laboratory screw

S4 045.4000 Aesthetic ProUnic® abutment. Hexed. Important: use specific instrumentation 1 mm, torque 25 Ncm.

All series of the ProUnic® Advance and ProUnic® product range have their colour code according to the series involved.

Aesthetic ProUnic® Non-hexed

Series Reference Designation

S3 042.3000 Aesthetic ProUnic® abutment. Non-hexed.

S4 042.4000 Titanium.

S3 044.3200 ProUnic® abutment non-hexed casting cylinder.

S4 044.4200 Aesthetic non-hexed for bridges and bars.

Plastic.

S3 043.3000 Titanium laboratory screw

S4 043.4000 Aesthetic ProUnic® abutment. Non-hexed.

S3 046.3000 Final titanium laboratory screw

S4 046.4000 Aesthetic ProUnic® abutment. Non-hexed.

Important: use specific instrumentation 1 mm, torque 25 Ncm.

All series of the ProUnic® Advance and ProUnic® product range have their colour code according to the series involved.

SCREWED RESTORATIONSAesthetic ProUnic® abutment

Heights, degrees and angles Aesthetic ProUnic®Aesthetic ProUnic® abutment. Hexed for single cases

with aesthetic involvement and scant vertical dimension.

· Aesthetic ProUnic® abutment. Hexed S3 · Height from implant shoulder: 2.1 mm

· Abutment conicity: 7º · Maximum angle between implants: 14º

· Aesthetic ProUnic® abutment. Hexed S4 · Height from implant shoulder: 2.4 mm · Abutment conicity: 7º · Maximum angle between implants: 14º

Aesthetic ProUnic® abutment. Non-hexed for

multiple restorations and bars.

· Aesthetic ProUnic® abutment. Non-hexed S3 · Height from implant shoulder: 1.7 mm

· Abutment conicity: 15º · Maximum angle between implants: 30º

· Aesthetic ProUnic® abutment. Non-hexed S4 · Height from implant shoulder: 2.0 mm · Abutment conicity: 15º · Maximum angle between implants: 30º

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Drillable abutments

Series Reference Designation

S3 038.3000 Internal abutment post without shoulder.

S4 038.4000 Hexed with screw.

S5 038.5000 Titanium.

S3 038.3100 Casting cylinder for internal abutment post.

S4 038.4100 Implant shoulder connection.

S5 038.5100 Plastic.

S3 038.3005 Hexed Abutment post.

S4 038.4005 Shoulder 0.5 mm with screw. Titanium.

S5 038.5005

S3 038.3015 Shoulder 1.5 mm.

S4 038.4015

S5 038.5015

S3 038.3030 Shoulder 3.0 mm

S4 038.4030

S3 021.3115 Angled Abutment post 15º. Hexed

S4 021.4115 with screw. Titanium.

S3 021.3125 Angled Abutment 25º.

S4 021.4125

S3 022.3115 Angled Abutment post 15º. Shoulder 1.0 mm.

S4 022.4115

S3 022.3125 Angled Abutment post 25º. Shoulder 1.0 mm.

S4 022.4125

CEMENTED RESTORATIONS Drillable Abutment Posts

OVERDENTURE RESTORATIONSLocator®

Locator®

Series Reference Designation

S3 1755 Locator® abutment. Height 1 mm. Titanium

S4 1761 Height 1.4 mm.

S3 1756 Height 2 mm.

S4 1762

S5 1767

S3 1757 Height 3 mm.

S4 1763

S3 1758 Height 4 mm.

S4 1764

S3 1759 Height 5 mm.

S4 1765

8519 Retention kit (2 units).

8540 Extended retention kit (2 units).

8514 Block out spacer (20 units.)

8393 Locator® tool.

8530 Analog (4 units).

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OVERDENTURE RESTORATIONSBall abutments

Delayed imprint transfer

Series Reference Designation

S3 011.3000 Impression coping - Direct implant.

S4 011.4000 With short screw: closed tray.

S5 011.5000 With long screw: open tray. Titanium.

S3 011.0003 Dual-Press®abutment.

S4 011.0045 Abutment for impression copings.

S5 011.0045 Titanium.

S3 011.3150 Dual-Press® Impression transfer.

S4 011.4150 Impression and Provisional millings copings.

S5 011.5100 Plastic.

Implant analogue

Series Reference Designation

S3 012.3000 Implant analog.

S4 012.4000 Titanium.

S5 012.5000

IMPRINTING

Ball abutments

Series Reference Designation

S3 022.3001* Ball abutment. Height 1 mm. Titanium.

S4 022.4001*

S3 022.3003* Height 3 mm.

S4 022.4003*

S3 022.3005* Height 5 mm.

S4 022.4005*

S3 022.0010 Ball abutment sleeve.

Titanium.

S3 022.0005 Ball abutment seal.

EPDM.

* Important: not indicated for restorations with angulation of over 30º.

OVERDENTURE RESTORATIONSLocator®

Locator®

Reference Designation

8505 Impression coping (4 units).

8517 Parallel post (4 units).

9530 Angulation guide.

Locator® is a registered trademark of Zest Anchors, Inc.

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Duplits

Series Reference Designation

S3 056.3001 Duplit® ProUnic® Advance.

S4 056.4001 Titanium.

S5 056.5001

S3 056.3110 Duplit® ProUnic® Advance. Titanium.

S4 056.4110 Transgingival 1.0 mm.

S5 056.5110

S3 056.3120 Transgingival 2.0 mm.

S4 056.4120

S3 056.3130 Transgingival 3.0 mm.

S4 056.4130

S3 029.3000 Duplit® ProUnic Plus®.

S4 029.4000 Titanium.

S5 029.5000

S3 030.3010 Duplit® ProUnic Plus®. Titanium.

S4 030.4010 Transgingival 1.0 mm.

S5 030.5010

S3 030.3020 Transgingival 2.0 mm.

S4 030.4020

S3 030.3030 Transgingival 3.0 mm.

S4 030.4030

S3 032.3000 Aesthetic Duplit® ProUnic ®. Hexed.

S4 032.4000 Titanium.

S3 033.3000 Aesthetic Duplit® ProUnic ®. Non-hexed.

S4 033.4000 Titanium.

S3 065.3000 Reamer for casting cylinders.

S4 065.4000 Available for abutment casting cylinders.

S5 065.5000 ProUnic Plus® and Aesthetic ProUnic® abutment.

Steel.

PLANNING ABUTMENTS

Planning instrumentation TSA® Advance

Reference Designation

102.0001 Radiographic template: 1:1 / 1.25:1 / 1.3:1

Plastic.

170.1000 Planning gauge.

Distance to implant indicator. Stainless.

170.2000 Open Guide® (4 units).

Titanium.

PLANNING INSTRUMENTS

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Reference Designation

171.0200 Surgical Box.

171.0200I Surgical Box Insert

171.0300T Surgical Box Lid

171.0300B Surgical Box Base

Surgical instrumentation TSA® Advance

Series Reference Designation

S3 150.0003 Circular scalpel for TSA® Advance.

S4 150.0004 Stainless.

S5 150.0005

Mechanical insertion for TSA® Advance

Reference Designation

173.0100 Contra-Angle Adapter, Short.

Connection: mounter. Stainless.

173.0300 Contra-Angle Adapter, Long.

Connection: mounter. Stainless.

173.1251 Contra-Angle Hex Driver, Short.

Connection: 1.25 mm. Stainless.

173.1252 Contra-Angle Hex Driver, Medium.

Connection: 1.25 mm. Stainless.

Manual insertion for TSA® Advance

Reference Designation

172.0000 Torque wrench.

Stainless.

172.0001 Open end wrench.

Titanium.

172.0100 Ratchet Adapter, Short - to Mounter.

Connection: mounter. Titanium.

172.0300 Ratchet Adapter, Long - to Mounter.

Connection: mounter. Titanium.

SURGICAL BOX

SURGICAL INSTRUMENTS

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Surgical instruments and prosthodontics 1.25

Reference Designation

174.1251 Manual Hex Driver, Short.

Connection: 1.25 mm. Stainless.

174.1252 Manual Hex Driver, Medium.

Connection: 1.25 mm. Stainless.

174.1253 Manual Hex Driver, Long.

Connection: 1.25 mm. Stainless.

172.1251 Hex Tool, Short - to Wrench.

Connection: 1.25 mm. Stainless.

172.1252 Hex Tool, Medium - to Wrench.

Connection: 1.25 mm. Stainless.

Prosthodontic instrumentation 1.0 | Aesthetic abutments

Reference Designation

174.1001 Manual Hex Driver, Short.

Connection: 1.0 mm. Stainless.

174.1002 Manual Hex Driver, Medium.

Connection: 1.0 mm. Stainless.

172.1001 Hex Tool, Short - to Wrench.

Connection: 1.0 mm. Stainless.

172.1002 Hex Tool, Medium - to Wrench.

Connection: 1.0 mm. Stainless.

173.1001 Contra-Angle Hex Driver, Short.

Connection: 1.0 mm. Stainless.

173.1002 Contra-Angle Hex Driver, Medium.

Connection: 1.0 mm. Stainless.

SURGICAL INSTRUMENTS

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SEQUENCE:

The planned depth and direction of implant insertion is established in the initial surgical drilling sequence.

Once initial drilling has been completed, we continue with the next sequences until final drilling corresponding to the planned implant diameter and

series - leaving the bone bed prepared for implant insertion.

IMPORTANT:

Insertion instruments with laser marking of depth.

The surgical drills are indicated for a maximum of 10 uses. Exceeding the indicated number of uses can adversely affect the success of

implant treatment.

Initial sequence TSA® Advance

Reference Designation

101.0001 Precision Drill.

Stainless.

175.1018 Round Marking Bur.

Dimensions: ø 1.8 mm. Stainless.

175.1023 Dimensions: ø 2.3 mm.

101.0323 Pilot Drill, Long.

Dimensions: ø 2.3 mm. Stainless.

101.0123 Pilot Drill, Short.

101.0000 Pilot Drill Parallelizer.

Dimensions: ø 2.3 mm. Titanium.

101.0328 Surgical Drill, Long.

Dimensions: ø 2.8 mm. Stainless.

101.0128 Surgical Drill, Short.

101.0028 Depth Indicator Drill.

Dimensions: ø 2.8 mm. Titanium.

SURGICAL INSTRUMENTS: INITIAL SEQUENCE

Supracrestal insertionThe TSA® Advance implant is designed to position the implant shoulder 0.7 mm above the bone crest, leaving this length of smooth neck as biological space for adhesion and sealing of the binding epithelium. The drilling length for implant insertion is the length of the implant minus 0.7 mm.

Further information on the surgical procedure is available at: www.defconimplants.com

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Final sequence TSA® Advance S3

Reference Designation

101.0330 Surgical Drill, Long.

Dimensions: ø 3.0 mm. Stainless.

101.0130 Surgical Drill, Short.

101.0030 Depth Indicator Drill.

Dimensions: ø 3.0 mm. Titanium.

101.1336* Contra-Angle Bone Tap, Long.

Manual via Ratchet Adapter,

Long ref. 172.0300.

Dimensions: ø 3.6 mm. Stainless.

101.1136* Contra-Angle Bone Tap, Short

Manual via Ratchet Adapter,

Long ref. 172.0300.

* Use in bone with type I-II bone quality.

Final sequence TSA® Advance S4

Reference Designation

101.0336 Surgical Drill, Long.

Dimensions: ø 3.6 mm. Stainless.

101.0136 Surgical Drill, Short.

101.0036 Depth Indicator Drill.

Dimensions: ø 3.6 mm. Titanium.

101.0342* Contra-Angle Bone Tap, Long.

Manual via Ratchet Adapter,

Long ref. 172.0300.

Dimensions: ø 4.2 mm. Stainless.

101.0142* Contra-Angle Bone Tap, Short

Manual via Ratchet Adapter,

Long ref. 172.0300.

* Use in bone with type I-II bone quality.

SURGICAL INSTRUMENTS: FINAL SEQUENCE

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Final sequence TSA® Advance S5

Reference Designation

101.0243 Surgical Drill, Short.

Dimensions: ø 4.3 mm. Stainless.

101.0249 Dimensions: ø 4.9 mm.

101.0043 Depth Indicator Drill.

Dimensions: ø 4.3 mm. Titanium.

101.0049 Dimensions: ø 4.9 mm.

101.0255* Contra-Angle Bone Tap.

Manual via Ratchet Adapter,

Long ref. 172.0300.

Dimensions: ø 5.5 mm. Stainless.

* Use in bone with type I-II bone quality.

SURGICAL INSTRUMENTS: FINAL SEQUENCE

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1. GENERAL SERVICE - We adapt to you.Client Service telephone 902 201 415 / 937 151 978 | Hours: Monday to Friday 9:00 a.m. to 1:30 p.m. and from 3:00 p.m. to 6:00 p.m. (except

holidays).

2. PRODUCT ORDERING - For your convenience, we have extended our office hours.Monday to Friday 9:00 a.m. to 1:30 p.m. and from 3:00 p.m. to 5:00 p.m. (except holidays) | Client Service telephone 902 201 415 / 937 151 978.

3. SUPPLY DEADLINES - We maintain the stock for you.· 24-48 h. Spanish peninsula (*) Deadlines according to reception of orders and office hours, as specified in section 2.

· 48-72 h. Insular (*) Deadlines according to reception of orders and office hours, as specified in section 2.

Exclusive for the current products of the DEFCON® implant system (except holidays).

4. SHIPPING OF PRODUCTS - For when you need them.Upon placing your order, tell us the type of service you require.

a) Delivery from 8:00 a.m. to 10:00 p.m.Monday to Friday.

b) Delivery after 10:00p.m. (*), according to shipping deadlines as specified in section 3. Monday to Friday.

(*) We cover the shipping and processing costs in section “b)” in the case of those material orders that equal or exceed 300 €, taxes not included.

5. PRODUCT RETURNSGiven the benefits derived from our products and sales conditions, returns will only be accepted of material pertaining to the

DEFCON® system in the 30 days following the invoice date, and provided the following conditions are met:

a) Before shipping the material, request the product return number from our Client Service, Tel. 902 201 415 / 937 151 978, and identify the material

along with the article code, amount and batch number.

b) All documents accompanying the merchandise, as well as the outer packaging, must state the number supplied by our Client Service.

c) Material not in perfect condition will not be accepted: there must be no opening, manipulation, marking or relabeling.

d) Having assigned the return number and received the material in our facilities, and following the pertinent quality controls, we will issue the

corresponding credit, to be compensated by future purchases.

e) The shipping costs associated with product return will be covered by the client.

f) Material from a commercial promotion invoiced by DEFCON® will not be admitted.

6. REPLACEMENT OF IMPLANTS AND PROSTHESESReplacements of DEFCON® products will be accepted during a maximum period of 12 months after the invoice date, provided the following

conditions are met:

a) Before shipping the material, request the product replacement number from our Client Service, and identify the material along with the article code,

amount and batch number.

b) Material not in perfect condition will not be accepted: there must be no damage, manipulation, marking or relabelling.

c) The material is to be shipped in protective packaging in order to avoid damage during shipment.

d) The costs of both reception and shipment, associated with product replacement, will be covered by the client.

7. INVOICING AND PAYMENT - Simple, AutomatisedDelivery notes and invoices will be automatically attached to the ordered product. The standard payment procedure is by bank account

30 days after the invoice date.

8. WE ARE INTERESTED IN YOUR OPINIONDEFCON Tissue Care® offers its clients an effective tool for contributing to the continued improvement of our services and products. If you inform

us of any incidents or comments, we can be much more effective. Our Client Service will enter your comments and observations in a special

client fidelisation program. We automatically activate a series of in-house processes to evaluate or reply to your comments. Your suggestions and

evaluations will be greatly appreciated.

Feedback is generated thanks to your cooperation, and allows us to take the opportune actions to ensure continuous improvement of our services:

for your full satisfaction.

· Taxes not included.

· DEFCON Tissue Care® and other brands of this catalogue are registered trademarks of Impladent, S.L.

· Impladent, S.L. reserves the right to modify the prices or products, or to correct mentions resulting from typographical errors, without prior warning.

This document was reviewed and approved on: 2010-10-18

Sales conditions

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Technological Center

P. I. Mas d’en Cisa.Gato Pérez, 3-908181 SentmenatBarcelona | SpainTel. +34 902 201 415Fax +34 902 259 260

www.defconimplants.com

REF.: CATTSADVEN_rev2

With you today and tomorrow.