Summary
Peri-implant disease (Mucositis and peri-implantitis) is a major and growing clinical problem in odontology, affecting 20-40
mill. patients in Europe, and the double worldwide. Labrida has developed, clinically documented and CE marked a novel,
patented (pending) maintenance device for non-surgical management of peri-implant disease. It is a revision brush
(“BioClean”), with bioresorbable bristles made of mono-filament chitosan fibres (Patented by Medovent, DE). It offers safer,
more effective, less painful and faster treatment of peri-implant disease, where currently the clinical community is in search
for adequate solutions. The instrument addresses a market in the range of Euro 1-2 billion annual turnover.
The device is in small scale production and sold commercially in Scandinavia (TRL 7), with most promising market response.
To meet the market opportunity, we will develop up-scaled production processes of advanced chitosan fibres, which is
critical to increase overall production requirements. In addition, we have started development with clinical pilot testing of the
next generation product, comprising chitosan bristles combined with antibiotics, with interesting clinical results. This may
open a broader application field for deployment of these combinations of materials technologies, both within odontology and
wider in medicine.
The overall planned project (Phase 2) comprises both industrial development of scaled up production technologies for the
chitosan fibres of the currently marketed product , as well as development of the next generation product, combining
advanced chitosan technologies with bioactive material, e.g. in nanospheres. In phase 1, we intend to refine the
development plan of these product(s) for phase 2, including assessing more in detail the business case, and additional
application areas, of the 2nd generation product.
mill. patients in Europe, and the double worldwide. Labrida has developed, clinically documented and CE marked a novel,
patented (pending) maintenance device for non-surgical management of peri-implant disease. It is a revision brush
(“BioClean”), with bioresorbable bristles made of mono-filament chitosan fibres (Patented by Medovent, DE). It offers safer,
more effective, less painful and faster treatment of peri-implant disease, where currently the clinical community is in search
for adequate solutions. The instrument addresses a market in the range of Euro 1-2 billion annual turnover.
The device is in small scale production and sold commercially in Scandinavia (TRL 7), with most promising market response.
To meet the market opportunity, we will develop up-scaled production processes of advanced chitosan fibres, which is
critical to increase overall production requirements. In addition, we have started development with clinical pilot testing of the
next generation product, comprising chitosan bristles combined with antibiotics, with interesting clinical results. This may
open a broader application field for deployment of these combinations of materials technologies, both within odontology and
wider in medicine.
The overall planned project (Phase 2) comprises both industrial development of scaled up production technologies for the
chitosan fibres of the currently marketed product , as well as development of the next generation product, combining
advanced chitosan technologies with bioactive material, e.g. in nanospheres. In phase 1, we intend to refine the
development plan of these product(s) for phase 2, including assessing more in detail the business case, and additional
application areas, of the 2nd generation product.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/672075 |
| Start date: | 01-06-2015 |
| End date: | 30-11-2015 |
| Total budget - Public funding: | 71 429,00 Euro - 50 000,00 Euro |
Cordis data
Original description
Peri-implant disease (Mucositis and peri-implantitis) is a major and growing clinical problem in odontology, affecting 20-40mill. patients in Europe, and the double worldwide. Labrida has developed, clinically documented and CE marked a novel,
patented (pending) maintenance device for non-surgical management of peri-implant disease. It is a revision brush
(“BioClean”), with bioresorbable bristles made of mono-filament chitosan fibres (Patented by Medovent, DE). It offers safer,
more effective, less painful and faster treatment of peri-implant disease, where currently the clinical community is in search
for adequate solutions. The instrument addresses a market in the range of Euro 1-2 billion annual turnover.
The device is in small scale production and sold commercially in Scandinavia (TRL 7), with most promising market response.
To meet the market opportunity, we will develop up-scaled production processes of advanced chitosan fibres, which is
critical to increase overall production requirements. In addition, we have started development with clinical pilot testing of the
next generation product, comprising chitosan bristles combined with antibiotics, with interesting clinical results. This may
open a broader application field for deployment of these combinations of materials technologies, both within odontology and
wider in medicine.
The overall planned project (Phase 2) comprises both industrial development of scaled up production technologies for the
chitosan fibres of the currently marketed product , as well as development of the next generation product, combining
advanced chitosan technologies with bioactive material, e.g. in nanospheres. In phase 1, we intend to refine the
development plan of these product(s) for phase 2, including assessing more in detail the business case, and additional
application areas, of the 2nd generation product.
Status
CLOSEDCall topic
NMP-25-2014-1Update Date
27-10-2022
Geographical location(s)
Structured mapping
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H2020-EU.2.1.2. INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies – Nanotechnologies
