DENTAL PRODUCT PORTFOLIO

DESU & LİNACOL MEDICAL GROUP

HAKKIMIZDA
DESU MEDIKAL, founded in 2007, is a medical research
and development company specialized in
neurotechnology.

By incorporating LINACOL MEDİKAL in 2014, we

transferred our experience and knowledge to the field of
orthopedics, oral and dental surgery and we continue to
develop innovative projects for medical device sector.

The headquarters of the company group are located in

Hacettepe University Technology Development Zone,
which aims to be the meeting point of advanced
technology, which hosts more than 300 national and
international companies.
NEDEN BİZ?

BAKIŞ AÇIMIZ
Müşterilerimize ve ortaklarımıza sunduğumuz çözümlerle gurur duyuyoruz.
Ortaklarımızı tanımak için çalışıyor ve her alanda destekliyoruz.
Kişiselleştirme, satış ve pazarlama tekniklerinde ilerici bir yaklaşım
benimsiyoruz.

İHTİYAÇLARINIZI ANLIYORUZ
Sektördeki deneyimimiz ve ekibimizin tıp alanındaki bilgi birikimi, bize
yenilikçi çözümler geliştirme konusunda avantaj sağlıyor. Taahhüdümüz,
ortaklarımıza ve müşterilerimize en iyi hizmeti ve yüksek kaliteli ürünleri
sunmaktır.

KALİTE POLİTİKAMIZ
Linacol ve Desu Medikal yetkin personeli ve üst düzey donanımıyla, ulusal
ve uluslararası standartlarda, müşteri gereksinimleri doğrultusunda gizlilik,
güvenilirlik ve izlenebilirlik ilkeleri temelinde kalite hedeflerini sürekli
geliştirerek, hatasız ve profesyonel hizmet vermeyi hedeflemekte ve
gerçekleştirmektedir.

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 MEDİKAL
DESU
XENOBONE®
COLLAGEN BASED ANIMAL
ORIGIN BONE SUBSTITUTE
XENOBONE® Collagen Based Animal Origin Bone
Substitute is a bioabsorbable, osteoconductive bone
matrix composed of Type-I Ultra-Pure Bovine Collagen
with ß-TCP adittion.

It is made from type-1 pure bovine achilles tendon

collagen which is one of the purest sources of
commercially available collagen. Source material is
sourced only from cattle sourced in compliance with
United States and European regulatory requirements.
Thanks to the ß-TCP additive, the mineralized part of the
biomaterial has an optimized porous structure that
provides the osteoconductive properties required for
bone filling.

Thanks to the Ultra-pure Type-I Bovine Collagen in its

content, it supports osteoconductive properties, while at
the same time, thanks to its osteoinductive properties, it
triggers bone regeneration and provides growth matrix
for osteoblasts.

XENOBONE® has an optimized microporous structure.

The implanted matrix maintains its position throughout
the healing period of the tissue, and it is completely bio-
absorbable.

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 MEDİKAL
DESU
COLLOS®
COLLAGEN BASED DURAL .

GRAFT
COLLOS® is a biocompatible collagen membrane barrier
produced from Ultra-Pure Type-I Bovine Collagen. While it
acts as a barrier in the areas it meets, it also supports tissue
regeneration thanks to its collagen content.

• With its optimum absorption and maximum regeneration

properties, it helps tissue and cell regeneration as well as its
barrier function.
• It maintains its flexible structure when interacting with body
fluids.
• It is easy to use. It allows double-sided use.
• It has high adhesion capacity. It can be used without sewing.
Due to its flexible and durable structure, it can be sewn when
desired.
• Thanks to its ergonomic and elastic structure, it has a
complex texture.
• It penetrates quickly and acts as a barrier.
• Biocompatible and completely resorbable in the body.
has structure.

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COLLOS® COLLAGEN BASED DURAL GRAFT

ERGONOMİK VE ELASTİK YAPISI SAYESİNDE KESİLEBİLİR,

BÜKÜLEBİLİR VE BÖLGEYE KOLAYCA UYGULANIR.
MEDİKAL
LINACOL

CUREOS®
ß-TCP / SILICATE
BONE GRAFT
CureOs®- Tricalcium Phosphate/Silicate Bone Graft is an
osteoconductive, 80% porous, resorbable and
biocompatible, FDA-approved bone substitute with
interconnected macroporous structure.

Thanks to the >95% ß-TCP and 1% Silicate it contains, it

strongly supports bone formation and accelerates bone
formation.

CureOs® provides the necessary structure for bone

growth and reproduction. It gives bone cells a way to
form new bone tissue.

After administration, CureOs® is slowly reabsorbed and

replaced by bone tissue within a maximum of 12 months.

CureOs® has pores from 1 to 550 microns in diameter

and >80% porosity that accelerates new bone formation
and increases osteoconductivity. Microporosity allows for
bone formation in the substitution and rapid spread of
bone-producing cells and increase of osteogenic cells
through osteoconduction.

It is completely biocompatible and osteogenic.

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MEDİKAL
LINACOL

CUREOS®
PUTTY INJECTABLE
ß-TCP BONE GRAFT
CureOs® Putty – is a bioabsorbable and biocompatible
osteoconductive bone substitute.

It accelerates bone growth and regeneration and

supports new bone formation.

After the application, the graft substitution is resorbed

and replaced by the bone tissue over time during the
healing process.

It can be mixed with bone marrow, blood and other

clinically known bone grafts.

Thanks to its minimal usage possibilities, it is frequently

preferred in oral, dental and maxillofacial surgery
operations.

It does not require long preparatory procedures. It saves

time and reduces risks for the patient.

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CUREOS® ß-TCP / SILICATE BONE GRAFT

MICROPOROUSITY ALLOWS BONE FORMATION IN SUBSTITUTE AND

PROVIDES RAPID SPREAD OF BONE PRODUCTION CELLS AND INCREASES
OF OSTEOGENIC CELLS THROUGH OSTEOCONDUCTION.
 ÜRÜN KODLARI VE AMBALAJ SEÇENEKLERİ

ÜRÜN KODU ÜRÜN ADI VE İÇERİĞİ
XBN-0715W-1CC XENOBONE Kolajen Bazlı
® CRS-05C-C01
Hayvansal Kaynaklı Kemik Grefti 0.7
- 1.5 mm, 1 cc - Granül
XBN-0715W-2CC XENOBONE® Kolajen Bazlı
Hayvansal Kaynaklı Kemik Grefti 0.7
- 1.5 mm, 2 cc - Granül
XBN-0715W-4CC XENOBONE® Kolajen Bazlı
Hayvansal Kaynaklı Kemik Grefti 0.7
- 1.5 mm, 4 cc - Granül
XBN-0715W-5CC XENOBONE Kolajen Bazlı
® Fosfat/Silikat Crunch Kemik Grefti
Hayvansal Kaynaklı Kemik Grefti 0.7
- 1.5 mm, 5 cc - Granül
XBN-23W-1CC XENOBONE® Kolajen Bazlı
Hayvansal Kaynaklı Kemik Grefti 2 -
3 mm, 1 cc - Granül
XBN-23W-2CC XENOBONE® Kolajen Bazlı
Hayvansal Kaynaklı Kemik Grefti 2 -
3 mm, 2 cc - Granül
XBN-23W-4CC XENOBONE® Kolajen Bazlı
Hayvansal Kaynaklı Kemik Grefti 2 -
3 mm, 4 cc - Granül
XBN-23W-5CC XENOBONE Kolajen Bazlı
® ß TCP Kemik Matrisi ,5 cc
Hayvansal Kaynaklı Kemik Grefti 2 -
3 mm, 5 cc - Granül
ÜRÜN KODU ÜRÜN ADI VE İÇERİĞİ
CureOs® > 95% Tri Kalsiyum
Fosfat/Silikat Crunch Kemik Grefti
İçerik:2-3 mm - 1 cc
CRS-05C-C01 CureOs® > 95% Tri Kalsiyum
Fosfat/Silikat Crunch Kemik Grefti
İçerik:2-3 mm - 1 cc
CRS-05C-C01 CureOs® > 95% Tri Kalsiyum
Fosfat/Silikat Crunch Kemik Grefti
İçerik:2-3 mm - 4 cc
CRS-05C-C01 CureOs® > 95% Tri Kalsiyum
İçerik:2-3 mm - 5 cc
CRS-PTY-001 CureOs® Steril Tek Kullanımlık
Hidroksiapatit Katkılı Enjekte Edilebilir
ß TCP Kemik Matrisi ,1 cc
CRS-PTY-002 CureOs® Steril Tek Kullanımlık
Hidroksiapatit Katkılı Enjekte Edilebilir
ß TCP Kemik Matrisi ,2 cc
CRS-PTY-003 CureOs® Steril Tek Kullanımlık
Hidroksiapatit Katkılı Enjekte Edilebilir
ß TCP Kemik Matrisi ,3 cc
CureOs® Steril Tek Kullanımlık
CRS-PTY-005 Hidroksiapatit Katkılı Enjekte Edilebilir

CLS2525 COLLOS® Kolajen Bazlı Dural Greft

2.5cm x 2.5cm – 2x (2.5cm x
1.25cm)

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 Klinik Vakalar
Case 1- Implant placement in the bone defect area after tooth extraction and grafting around the implant

1 2 3 4

BEFORE 6 MONTHS LATER

Case 2 - Sinus Sagging in the Left Upper Jaw - Closed Sinus Lift Graft and Implant Application

1 2 3

1. Initial 3mm Crestal Bone

2. 8.5mm implant placement with Closed Sinus Lift Technique
3. 8.5mm Crestal Bone (5.5mm long new bone formation) after 6 months

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 3. Case 4. Case

1 2 1 2

1. Impacted tooth and extraction indication in the right upper jaw 1. Sinus prolapse due to edentulism and infected area in the right upper
2. post-procedure graft and implant placement jaw
2. 3rd month view after 11.5mm implant placement with open sinus lift
and graft application

Case 5 - Large bone defects in the lower and upper jaw - Graft and implant application

1 2 3

New bone formation and osseointegrated implants

after 6 months

6. Case

1 2 3

1. With edentulousness in the left upper jaw and sinus sagging

2. Placement of 10mm long implant with closed sinus lift (Graft materials are observed
around the implant)
3. Bone formation around the implant at the end of 6 months

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 CONTACT INFORMATION

DESU MEDİKAL ÜRÜNLERİ VE TIBBİ CİHAZLAR SAN. VE TİC. A.S.

Merkez: Üniversiteler Mah. 1596 Cad. Hacettepe Teknokent Safir Bina
E Blok Zemin Kat - Çankaya, Ankara / Türkiye
Telefon: +90 312 299 25 63
www.desumedical.com.tr

LİNACOL MÜHENDİSLİK DAN.KİM.ÇEV.TEK. MEDİKAL İTH.İHR.SAN. VE TİC.LTD.ŞTİ

Merkez: Üniversiteler Mah. 1596 Cad. Hacettepe Teknokent Safir Bina E Blok
Zemin Kat - Çankaya, Ankara / Türkiye
Telefon: +90 312 299 25 63
www.linacolmedikal.com