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COMPANY OVERVIEW
1 | P a g e
Veritas Bioventions is a leader in the design and development of innovative
medical devices. Our devices help patients with vascular & dental disorders to
return to active and productive lives. We provide physicians with leading-edge
technologies for improved patient management and clinical outcomes. We offer
products, therapies and services that will enhance or extend lives of people
worldwide. Veritas Bioventions was incorporated in 2009; corporate headquarter
is in India, with major operations worldwide. A sales force recognized
throughout the industry for its clinical expertise and customer service insight to
distribute our products.
Continued honest and ethical business conduct has earned Veritas Bioventions
the trust of customers, patients, suppliers, investors, regulators, and fellow
employees, while sustaining our long-term commitment to physicians.
As such, we are committed to being an innovative, unique, world-class
corporation. The only way we achieve this commitment is by providing a high
standard of leadership, along with unquestionable corporate integrity. Our
structure provides the resources of a large organization. The business groups stay
close to the customer and respond quickly to evolving needs. They advance the
organization’s mission of providing leading-edge technology for physicians and
life-saving therapy for patients. At Veritas Bioventions, we believe that advanced
technologies can provide solutions for unmet clinical needs. That's why we work
hard to stimulate a continual stream of innovation in the medical technology
industry.
Vision & Mission
Veritas Bioventions mission is to improve the quality of patient care and the
productivity of health care delivery through the development and advocacy of
less-invasive medical devices and procedures. This is accomplished through the
continuing refinement of existing product and procedures and the investigation
and development of new technologies which can reduce risk, trauma, cost,
procedure time and the need for aftercare.
COMPANY OVERVIEW
2 | P a g e
Research and Development
Veritas Bioventions is an advanced stage, research and development company
pursuing the commercialization of the next generation of fully biocompatible
coating for Stents (biocompatible, non-toxic, non-thrombogenic, non-
inflammatory & highly angiogenic) and cutting edge technology for DES. Veritas
Bioventions has engineered a process to produce a carrier that can carry many
classes of therapeutic agents. The projects on DES will address all the
shortcomings of the present commercially available DES. We have also
pioneered in the field of polymer free coating technology in DES with more than
five different proprietary coating technology which are in progress & which will
also address all the future complication of present DES of late thrombosis.
Veritas Bioventions is also working on active drug delivery systems that can
deliver varying combinations and doses of many therapeutic agents including
large and small molecules, proteins, peptides and Genes.
Veritas Bioventions is a milestone ahead in developing a versatile implant
system fulfilling demands of contemporary implantology. We will continue to
lead the dental industry in implant, restorative, regenerative, and digital dentistry
solutions. We remain focused on research and development initiatives that will
improve patient’s quality of life, dentistry will continue to migrate towards more
and more digital solutions for the end benefit of the patient. We will continue to
develop new products that meet the needs of our customers and their patients.
Veritas Bioventions is developing a new implant bio- material made of
zirconium and titanium. Its tensile strength is 60% greater than pure Grade 4
titanium and designed for use in small-diameter implants in narrow interdental
spaces. For clinicians, this new patented bio-material will offer greater
confidence while placing small-diameter implants and the flexibility of having
more treatment options.
Surface chemistry has the potential to alter ionic interaction, protein adsorption,
and cellular activity at the implant surface. These modifications may
subsequently influence conformational changes in the structures and interactive
natures of adsorbed proteins and cells. Furthermore, within the complexities of an
in vivo environment containing multiple protein and cellular interactions, these
COMPANY OVERVIEW
3 | P a g e
alterations may differentially regulate biologic events. Hence Veritas
Biovention’s chemically modified sLa surface is in a development phase to
address unmet clinical needs in modern dentistry.
Our present available product range includes:
 Enovo
Everolimus Eluting Coronary Stent on Cobalt Chromium L605
Platform mounted on Rapid Exchange delivery system
The Enovo Coronary Stent System includes loading and elusion of
Everolimus Drug in a controlled fashion on L605 Cobalt
Chromium (Co – Cr alloy) Platform, stent located on balloons
catheter between two platinum iridium radio opaque markers
bands. The drug is encapsulated with several biodegradable
polymers and loaded on the stent through a proprietary coating
technology.
The Enovo is indicated for improving coronary luminal diameter in
patients with symptomatic ischemic heart disease in de novo
coronary artery lesion in native coronary arteries with a reference
vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40
mm. The Enovo is intended for use in patients eligible for
Percutaneous Transluminal Coronary Angioplasty (PTCA).
COMPANY OVERVIEW
4 | P a g e
 Sinew
Sirolimus Eluting Coronary Stent on Cobalt Chromium L605
Platform mounted on Rapid Exchange delivery system
The Sinew Coronary Stent System includes loading and elusion of
Sirolimus Drug in a controlled fashion on L605 Cobalt Chromium
(Co – Cr alloy) Platform, stent located on balloons catheter
between two platinum iridium radio opaque markers bands. The
drug is encapsulated with several biodegradable polymers and
loaded on the stent through a proprietary coating technology.
The Sinew is indicated for improving coronary luminal diameter in
patients with symptomatic ischemic heart disease in de novo
coronary artery lesion in native coronary arteries with a reference
vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40
mm. The Sinew is intended for use in patients eligible for
Percutaneous Transluminal Coronary Angioplasty (PTCA).
 Inspire
Paclitaxel Eluting Coronary Stent on Cobalt Chromium L605
Platform mounted on Rapid Exchange delivery system
The Inspire Coronary Stent System includes loading and elusion of
Paclitaxel Drug in a controlled fashion on L605 Cobalt Chromium
(Co – Cr alloy) Platform, stent located on balloons catheter
between two platinum iridium radio opaque markers bands. The
drug is encapsulated with several biodegradable polymers and
loaded on the stent through a proprietary coating technology.
The Inspire is indicated for improving coronary luminal diameter
in patients with symptomatic ischemic heart disease in de novo
coronary artery lesion in native coronary arteries with a reference
vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40
mm. The Inspire is intended for use in patients eligible for
Percutaneous Transluminal Coronary Angioplasty (PTCA).
COMPANY OVERVIEW
5 | P a g e
 Endorser Coronary Stent System
Stainless Steel SS316L Stent mounted on Rapid Exchange delivery
system
The Endorser Coronary Stent System includes 316L Stainless Steel
Stent located on balloons catheter between two platinum iridium
radio opaque markers bands. The Endorser stent is indicated for
improving coronary luminal diameter in patients with symptomatic
ischemic heart disease in de novo coronary artery lesion in native
coronary arteries with a reference vessel diameter of 2.25 mm to
4.0 mm and a lesion length  40 mm. The Endorser is intended for
use in patients eligible for Percutaneous Transluminal Coronary
Angioplasty (PTCA). This latest generation design of Endorser
has a unique geometry for controlled & distinctive stent expansion
which enables low stent induced mechanical injury to arterial wall
and excellent vessel conformability.
 Endorser CrCo Coronary Stent System
Cobalt Chromium L605 Stent mounted on Rapid Exchange delivery
system
The Endorser CrCo coronary stent System includes L605 Cobalt
Chromium (Co – Cr alloy) stent located on balloons catheter
between two platinum iridium radio opaque markers bands.
The Endorser CrCo is indicated for improving coronary luminal
diameter in patients with symptomatic ischemic heart disease in de
novo coronary artery lesion in native coronary arteries with a
reference vessel diameter of 2.25 mm to 4.0 mm and a lesion
length  40 mm. The Endorser CrCo is intended for use in patients
eligible for Percutaneous Transluminal Coronary Angioplasty
(PTCA).
COMPANY OVERVIEW
6 | P a g e
 Escalate
Inflation Device with / without three way stop-cock
Escalate Disposable Inflation Device is a sterile 30 ATM inflation
devices with a spring loaded Trigger Locking mechanism which is
easy to operate even with wet hands.
The Pressure gauge marking is specially designed for easy pressure
monitoring and fatigue free viewing during the procedure.
 Console
Y-Connector + Guide wire Insertion Tool + Torquer
CONSOLE is a 7.2 Fr device, which is used for coronary
intervention. It has a latest Push –Pull head knob, which ensures
minimal blood and precise navigation of devices in the vasculature.
A specially engineered valve with micro vertical slits which
facilitate smooth manipulation of device and nullify blood loss.
INSERTION TOOL: It is precisely designed for use during
Percutaneous Transluminal Coronary Angioplasty (PTCA) and any
other intravascular therapeutic procedures that utilize a guide wire.
Stainless Steel tube inner ID is 0.60 mm and Hub ID is 0.55 mm,
which provides smooth and resistance free movement of the guide
wire through the hub.
GUIDE WIRE TORQUER provides a mean for maneuvering
guide wires once inserted deep into the vasculature. The brass
collate inside the Torquer can comply to manure guide wires from
0.043” to 0.050”.
COMPANY OVERVIEW
7 | P a g e
 WaneCore Dental Implant
WaneCore dental implant is a root-form endosseous implant
system designed to mimic the shape of the tooth for directional
load distribution. WaneCore dental implant is indicated for
surgical placement in the upper or lower jaw arches, to provide a
root form means for single or multiple units’ prosthetic appliance
attachments to restore patient’s chewing function. Implant can be
placed with conventional two stage surgical process with an option
for transmucosal healing or they can be placed in single stage
surgical process for immediate loading.
WaneCore Dental implant has micro channels on the collar,
custom made threads are incorporated on the body of the implant,
have modified surface and a conical connection for post restorative
attachments. Three self tapping groves are given on the apical end
of the implant.
HIGHLIGHTS
Implant design (WaneCore): Parallel wall cylindrical with apical
taper having self tapping micro channels at crestal level for
increased primary stability.
Implant design (WaneCoreXP): Dual tapper implant design with
self cutting deep threads, reverse taper at the neck for bone
preservation, high primary stability in poor bone conditions.
Surface texture: SLA surface for greater BIC (Bone Implant
Contact) & enhanced Osseointegration.
Connection: Conical connection with platform switching benefits
for multiple prosthetic options.
COMPANY OVERVIEW
8 | P a g e
 WaneCore Prosthetics
WaneCore Dental Implant system consist of variety of prosthetic
component, all components are manufactured from Biocompatible
grade Titanium Alloy (Ti-6Al-4V Eli), gives various options to the
dentist during the restorative work.
The prosthetic components mainly contain Gingiava Formers for
aesthetic soft tissue integration around the crown, Solid and Hollow
Abutments with wide range of collar heights, Angled Abutments,
UCLA Abutments, Castable abutments and Multi unit abutments for
single or multiple unit’ restoration and Ball overdenture attachments
for full mouth restorations. Transfer coping for open and close tray
technique along with Implant analog.
 WaneCore Surgical Kit
WaneCore Dental Implant system consists of complete surgical kit
& Hybrid Surgical Kit.
WaneCore surgical Kit mainly consist all length & diameters of
Surgical drills for cavity preparation, Parallel Pins and Depth gauge
for accurate cavity measurements, various Implant drivers for
Surgical placement of Dental implant in to the cavity and Adjustable
Torque Wrench for implant placement at various forces.
Individual surgical drills are provided for individual length of the
implant which provides precise and accurate cavity preparation for
implant placement.
COMPANY OVERVIEW
9 | P a g e
All surgical drills are laser marked for the easy identification and
manufactured from surgical grade stainless steel with higher
hardness and corrosion resistance properties, these drills are further
coated with DLC coating to increase the life and cutting efficiency
of the drills.
All these surgical kit components are provided in sterilizable
surgical tray with well define color coding and laser marking for
easy identification of all the components.

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Veritas Bioventions Company Overview

  • 1. COMPANY OVERVIEW 1 | P a g e Veritas Bioventions is a leader in the design and development of innovative medical devices. Our devices help patients with vascular & dental disorders to return to active and productive lives. We provide physicians with leading-edge technologies for improved patient management and clinical outcomes. We offer products, therapies and services that will enhance or extend lives of people worldwide. Veritas Bioventions was incorporated in 2009; corporate headquarter is in India, with major operations worldwide. A sales force recognized throughout the industry for its clinical expertise and customer service insight to distribute our products. Continued honest and ethical business conduct has earned Veritas Bioventions the trust of customers, patients, suppliers, investors, regulators, and fellow employees, while sustaining our long-term commitment to physicians. As such, we are committed to being an innovative, unique, world-class corporation. The only way we achieve this commitment is by providing a high standard of leadership, along with unquestionable corporate integrity. Our structure provides the resources of a large organization. The business groups stay close to the customer and respond quickly to evolving needs. They advance the organization’s mission of providing leading-edge technology for physicians and life-saving therapy for patients. At Veritas Bioventions, we believe that advanced technologies can provide solutions for unmet clinical needs. That's why we work hard to stimulate a continual stream of innovation in the medical technology industry. Vision & Mission Veritas Bioventions mission is to improve the quality of patient care and the productivity of health care delivery through the development and advocacy of less-invasive medical devices and procedures. This is accomplished through the continuing refinement of existing product and procedures and the investigation and development of new technologies which can reduce risk, trauma, cost, procedure time and the need for aftercare.
  • 2. COMPANY OVERVIEW 2 | P a g e Research and Development Veritas Bioventions is an advanced stage, research and development company pursuing the commercialization of the next generation of fully biocompatible coating for Stents (biocompatible, non-toxic, non-thrombogenic, non- inflammatory & highly angiogenic) and cutting edge technology for DES. Veritas Bioventions has engineered a process to produce a carrier that can carry many classes of therapeutic agents. The projects on DES will address all the shortcomings of the present commercially available DES. We have also pioneered in the field of polymer free coating technology in DES with more than five different proprietary coating technology which are in progress & which will also address all the future complication of present DES of late thrombosis. Veritas Bioventions is also working on active drug delivery systems that can deliver varying combinations and doses of many therapeutic agents including large and small molecules, proteins, peptides and Genes. Veritas Bioventions is a milestone ahead in developing a versatile implant system fulfilling demands of contemporary implantology. We will continue to lead the dental industry in implant, restorative, regenerative, and digital dentistry solutions. We remain focused on research and development initiatives that will improve patient’s quality of life, dentistry will continue to migrate towards more and more digital solutions for the end benefit of the patient. We will continue to develop new products that meet the needs of our customers and their patients. Veritas Bioventions is developing a new implant bio- material made of zirconium and titanium. Its tensile strength is 60% greater than pure Grade 4 titanium and designed for use in small-diameter implants in narrow interdental spaces. For clinicians, this new patented bio-material will offer greater confidence while placing small-diameter implants and the flexibility of having more treatment options. Surface chemistry has the potential to alter ionic interaction, protein adsorption, and cellular activity at the implant surface. These modifications may subsequently influence conformational changes in the structures and interactive natures of adsorbed proteins and cells. Furthermore, within the complexities of an in vivo environment containing multiple protein and cellular interactions, these
  • 3. COMPANY OVERVIEW 3 | P a g e alterations may differentially regulate biologic events. Hence Veritas Biovention’s chemically modified sLa surface is in a development phase to address unmet clinical needs in modern dentistry. Our present available product range includes:  Enovo Everolimus Eluting Coronary Stent on Cobalt Chromium L605 Platform mounted on Rapid Exchange delivery system The Enovo Coronary Stent System includes loading and elusion of Everolimus Drug in a controlled fashion on L605 Cobalt Chromium (Co – Cr alloy) Platform, stent located on balloons catheter between two platinum iridium radio opaque markers bands. The drug is encapsulated with several biodegradable polymers and loaded on the stent through a proprietary coating technology. The Enovo is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40 mm. The Enovo is intended for use in patients eligible for Percutaneous Transluminal Coronary Angioplasty (PTCA).
  • 4. COMPANY OVERVIEW 4 | P a g e  Sinew Sirolimus Eluting Coronary Stent on Cobalt Chromium L605 Platform mounted on Rapid Exchange delivery system The Sinew Coronary Stent System includes loading and elusion of Sirolimus Drug in a controlled fashion on L605 Cobalt Chromium (Co – Cr alloy) Platform, stent located on balloons catheter between two platinum iridium radio opaque markers bands. The drug is encapsulated with several biodegradable polymers and loaded on the stent through a proprietary coating technology. The Sinew is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40 mm. The Sinew is intended for use in patients eligible for Percutaneous Transluminal Coronary Angioplasty (PTCA).  Inspire Paclitaxel Eluting Coronary Stent on Cobalt Chromium L605 Platform mounted on Rapid Exchange delivery system The Inspire Coronary Stent System includes loading and elusion of Paclitaxel Drug in a controlled fashion on L605 Cobalt Chromium (Co – Cr alloy) Platform, stent located on balloons catheter between two platinum iridium radio opaque markers bands. The drug is encapsulated with several biodegradable polymers and loaded on the stent through a proprietary coating technology. The Inspire is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40 mm. The Inspire is intended for use in patients eligible for Percutaneous Transluminal Coronary Angioplasty (PTCA).
  • 5. COMPANY OVERVIEW 5 | P a g e  Endorser Coronary Stent System Stainless Steel SS316L Stent mounted on Rapid Exchange delivery system The Endorser Coronary Stent System includes 316L Stainless Steel Stent located on balloons catheter between two platinum iridium radio opaque markers bands. The Endorser stent is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40 mm. The Endorser is intended for use in patients eligible for Percutaneous Transluminal Coronary Angioplasty (PTCA). This latest generation design of Endorser has a unique geometry for controlled & distinctive stent expansion which enables low stent induced mechanical injury to arterial wall and excellent vessel conformability.  Endorser CrCo Coronary Stent System Cobalt Chromium L605 Stent mounted on Rapid Exchange delivery system The Endorser CrCo coronary stent System includes L605 Cobalt Chromium (Co – Cr alloy) stent located on balloons catheter between two platinum iridium radio opaque markers bands. The Endorser CrCo is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length  40 mm. The Endorser CrCo is intended for use in patients eligible for Percutaneous Transluminal Coronary Angioplasty (PTCA).
  • 6. COMPANY OVERVIEW 6 | P a g e  Escalate Inflation Device with / without three way stop-cock Escalate Disposable Inflation Device is a sterile 30 ATM inflation devices with a spring loaded Trigger Locking mechanism which is easy to operate even with wet hands. The Pressure gauge marking is specially designed for easy pressure monitoring and fatigue free viewing during the procedure.  Console Y-Connector + Guide wire Insertion Tool + Torquer CONSOLE is a 7.2 Fr device, which is used for coronary intervention. It has a latest Push –Pull head knob, which ensures minimal blood and precise navigation of devices in the vasculature. A specially engineered valve with micro vertical slits which facilitate smooth manipulation of device and nullify blood loss. INSERTION TOOL: It is precisely designed for use during Percutaneous Transluminal Coronary Angioplasty (PTCA) and any other intravascular therapeutic procedures that utilize a guide wire. Stainless Steel tube inner ID is 0.60 mm and Hub ID is 0.55 mm, which provides smooth and resistance free movement of the guide wire through the hub. GUIDE WIRE TORQUER provides a mean for maneuvering guide wires once inserted deep into the vasculature. The brass collate inside the Torquer can comply to manure guide wires from 0.043” to 0.050”.
  • 7. COMPANY OVERVIEW 7 | P a g e  WaneCore Dental Implant WaneCore dental implant is a root-form endosseous implant system designed to mimic the shape of the tooth for directional load distribution. WaneCore dental implant is indicated for surgical placement in the upper or lower jaw arches, to provide a root form means for single or multiple units’ prosthetic appliance attachments to restore patient’s chewing function. Implant can be placed with conventional two stage surgical process with an option for transmucosal healing or they can be placed in single stage surgical process for immediate loading. WaneCore Dental implant has micro channels on the collar, custom made threads are incorporated on the body of the implant, have modified surface and a conical connection for post restorative attachments. Three self tapping groves are given on the apical end of the implant. HIGHLIGHTS Implant design (WaneCore): Parallel wall cylindrical with apical taper having self tapping micro channels at crestal level for increased primary stability. Implant design (WaneCoreXP): Dual tapper implant design with self cutting deep threads, reverse taper at the neck for bone preservation, high primary stability in poor bone conditions. Surface texture: SLA surface for greater BIC (Bone Implant Contact) & enhanced Osseointegration. Connection: Conical connection with platform switching benefits for multiple prosthetic options.
  • 8. COMPANY OVERVIEW 8 | P a g e  WaneCore Prosthetics WaneCore Dental Implant system consist of variety of prosthetic component, all components are manufactured from Biocompatible grade Titanium Alloy (Ti-6Al-4V Eli), gives various options to the dentist during the restorative work. The prosthetic components mainly contain Gingiava Formers for aesthetic soft tissue integration around the crown, Solid and Hollow Abutments with wide range of collar heights, Angled Abutments, UCLA Abutments, Castable abutments and Multi unit abutments for single or multiple unit’ restoration and Ball overdenture attachments for full mouth restorations. Transfer coping for open and close tray technique along with Implant analog.  WaneCore Surgical Kit WaneCore Dental Implant system consists of complete surgical kit & Hybrid Surgical Kit. WaneCore surgical Kit mainly consist all length & diameters of Surgical drills for cavity preparation, Parallel Pins and Depth gauge for accurate cavity measurements, various Implant drivers for Surgical placement of Dental implant in to the cavity and Adjustable Torque Wrench for implant placement at various forces. Individual surgical drills are provided for individual length of the implant which provides precise and accurate cavity preparation for implant placement.
  • 9. COMPANY OVERVIEW 9 | P a g e All surgical drills are laser marked for the easy identification and manufactured from surgical grade stainless steel with higher hardness and corrosion resistance properties, these drills are further coated with DLC coating to increase the life and cutting efficiency of the drills. All these surgical kit components are provided in sterilizable surgical tray with well define color coding and laser marking for easy identification of all the components.