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FMSi — Fortschritt Medical Supplies Inc.
PH-FDA: CMDR-2025-04943B

FlexiOss® Dent

Modern implantable biomaterial for dental and maxillofacial procedures. Available in 1cm, 3cm, and 5cm sizes.

Third-generation biphasic (hydroxyapatite-polymeric) biomaterial, bioactive, supporting bone tissue regeneration. After implantation, it integrates with the patient's bone and is slowly remodelled into natural bone tissue — eliminating the need for reoperation.

FlexiOss Dent — PH-FDA certified biphasic biomaterial for dental maxillofacial bone augmentation and socket preservation
1cm3cm5cm

Product Demonstrations

FlexiOss® Dent — Easy & Effective Bone Matrix

Product overview showcasing the dental bone filler properties, flexibility, and clinical applications.

FlexiOss® — Clinical Application

Clinical demonstration of FlexiOss® in dental procedures including socket preservation and bone augmentation.

Innovative Properties

What Makes FlexiOss® Dent Unique

01

Flexible After Soaking

Plastic and bendable — fits individual bone defects by cutting or bending

02

Bio-Compatible

Compatible with natural bone tissue for seamless integration

03

Mechanical Parameters

Similar to those of cancellous bone — structural support

04

Supports Bone Reconstruction

Actively supports the bone reconstruction process

05

Absorbs Blood & Medicine

High soaking capacity for enhanced drug delivery

06

Bone Tissue Regeneration

Positively affects bone tissue regeneration process

07

Ionic Reactive / Bioactive

High ionic reactivity increases mineralization rate

08

Non-Toxic Material

Thoroughly tested for safety — no cytotoxicity

09

Up to 7cm Defects

Can be used for bone defects of up to 7 cm in length

10

Non-Animal Material

Lowers risk of pathogen transmission and allergic reactions

11

Easy to Store & Transport

Simple storage and transportation requirements

Surgical Advantages

01

Surgical Handiness

Allows fitting during operation to the shape of individual bone defects by cutting or bending.

02

Can Be Milled

In dry state, FlexiOss® Dent can be milled for personalized composite implants.

03

Faster Ossification

High specific surface area and ionic reactivity increases mineralization rate and new bone formation.

04

Minimizes Contamination Risk

Curdlan polymer minimizes virus/prion risk. Forms collagen-like triple helix neutral to macrophages.

05

High Soaking Capacity

Can be soaked in antibacterial drugs, PRP, or growth factors, resembling expensive BMP-2-type substitutes.

06

Barrier Function

Helps prevent the migration of soft-tissue cells into the bone defect. Used standalone or combined with other grafting materials.

07

Easy Storage & Transport

No special conditions needed. Simple logistics for clinics worldwide.

Maxillofacial Applications

FlexiOss® Dent vs BonAlive®

A side-by-side against S53P4 bioactive glass granules for cranio-maxillofacial reconstruction. Every figure is drawn from each manufacturer's own published documentation.

FlexiOss Dent compared with BonAlive Granules for maxillofacial applications
AttributeFlexiOss® DentBonAlive® Granules / CMF
Product formPre-formed sterile cylinder in a double paper-foil pack, ready to placeBioactive glass granules in an individually packaged, pre-filled syringe
Available sizesØ13 mm cylinder in 1 cm, 3 cm and 5 cm lengthsGranules: 1cc, 2.5cc, 5cc, 10cc. CMF: 2.5cc, 5cc
CompositionHAP granules (>100 nm) bound with curdlan, a β-1,3 glucan sugar polymerS53P4 bioactive glass: 53% SiO₂, 23% Na₂O, 20% CaO, 4% P₂O₅
PorosityMicro and macroporous, ~30 µm pores, 68 to 70% porositySolid granules. Porosity is limited to the inter-granular space plus a surface hydroxyapatite layer
Handling & absorptionAbsorbs blood and plasma, becoming malleable and trimmable during surgeryDoes not absorb fluids. Moistened with saline before implantation. Volume and weight stay unchanged
Intraoperative preparationReady out of pack, no lengthy preparationRequires saline injection into the granule syringe and spatula assembly
Intraoperative safetyNo loose granules to migrate, no glove-puncture riskDisplaced granules can abrade nearby articular surfaces. Granules can puncture surgical gloves, a contamination risk
OsteoconductivityOsteoconductive scaffold with strong osseointegration, supports vascularisationOsteoconductive and osteostimulating (non-osteoinductive)
ResorbabilityHAP resorbs. Curdlan degrades to glucose that enters normal metabolismForms a silica gel layer that crystallises to resorbable hydroxyapatite, replacing bone over several years
Animal or human tissueNoneNone
Immunological / toxic reactionNoneContraindicated in patients allergic to bioactive glass
SterilisationEthylene oxideIrradiation
X-ray visibilityYesYes, also visible on CT and MRI
IndicationsSmall and large cavities across orthopedics, traumatology, dental and veterinary surgeryCranio-maxillofacial (mandible, frontal-sinus and mastoid obliteration, nasal-cavity narrowing). Also orthopedic cavity and osteomyelitis filling

Comparison drawn from Medical Inventi S.A. and Bonalive Biomaterials Ltd. manufacturer documentation (BonAlive® Granules and Granules CMF Instructions For Use). Provided for clinical reference.

01

No lengthy preparation

FlexiOss® is ready to place straight from the pack. BonAlive® requires saline to be injected into the granule syringe and a spatula assembled before use.

02

No granule migration

FlexiOss® stays where it is placed. Loose BonAlive® granules can travel beyond the implanted area and abrade nearby articular surfaces, impeding movement.

03

No glove-puncture risk

The cohesive FlexiOss® cylinder carries no puncture hazard. BonAlive® granules can perforate surgical gloves, introducing a microbiological contamination risk.

04

Delivered EO-sterile

FlexiOss® is sterilised with ethylene oxide and supplied to the customer ready for the operating field.

PhilHealth Coverage

PhilHealth Subsidy & Co-Payment Guide

Understand your PhilHealth subsidy allowance and co-payment options for procedures that use FlexiOss® — written for both patients and clinicians.

View PhilHealth Codes
TRICUREAN COMPOSITION

Biphasic Formula

Biphasic (hydroxyapatite-polymeric) composite obtained by polymer gelling into an irreversible, collagen-like triple helix — neutral for macrophages, no local inflammation.

Hydroxyapatite (HAP)

Ceramic Phase

Low-sintered, highly porous ceramic

Fully synthetic — high chemical stability

Active bone regeneration via ion uptake

Curdlan Polymer

Polymeric Phase

Triple-helix (collagen-like) structure

Non-inflammatory conformation

Enables flexibility & high absorbency

DENTAL APPLICATIONS

Clinical Uses

01

Post-extraction alveolar bone augmentation

02

Dental implant site preparation and preservation

03

Maxillofacial reconstructive procedures

04

Treatment of gingival resection with bone atrophy

05

Filling defects after cystotomy and root resection

06

Oronasal fistulae treatment and closure

07

Open socket preservation without membrane

08

Bioactive filling of titanium scaffolds in implantology

09

Treatment of dental cysts

10

Interdental bone tissue regeneration

11

Mastoid cavity obliteration following cholesteatoma surgery (tympanomastoidectomy)

12

Temporal-bone / skull-base defect filling after cerebellopontine angle (CPA) tumor excision

Available Sizes

1 cm (small defects)3 cm (medium defects)5 cm (large defects)

Certifications & Patents

CE

CE Certified

EC No. 1434-MDD-269/2021

European conformity — highest safety standards

FDA

PH-FDA Approved

CMDR-2025-04943B

Certified for dental & maxillofacial applications in the Philippines

PAT

Patent Protected

European Patents

Protected across England, Austria, France, Spain, Ireland, Germany, Poland & Italy

AWARDS & RECOGNITION

International Recognition

The FlexiOss® technology and its inventors have been recognised by leading scientific and intellectual-property institutions.

2013

Best Invention by a Woman Inventor

World Intellectual Property Organization (WIPO / OMPI)

2016

Prix Galien Poland, Innovative Scientific Discovery

Prix Galien Foundation

2019

Economic Award of the President of Poland, Research & Development

Office of the President of the Republic of Poland

2019

Future Product of the Entrepreneur

21st Polish Future Product Competition

Developed and manufactured by Medical Inventi S.A. (Poland). Exclusively distributed in the Philippines by Fortschritt Medical Supplies Inc.

CLINICAL EVIDENCE

Documented Results

Oronasal Fistula Treatment

Cat oronasal fistula filling procedure with X-ray evaluation directly after implantation and 1 month post-op showing positive integration.

Canine Oronasal Fistula

Dog oronasal fistula filling — removal of luxated canine tooth and filling of the fistula with FlexiOss® Dent biomaterial.

Bone Density Progression

MicroCT (pQCT) evaluation showing bone density increase from implantation through 1, 3, and 6 months — confirming progressive bone formation.

Histological Integration

Histological images confirming bone cells, laminae, collagen fibres and Haversian canals at implantation site — unequivocal bone tissue formation.

Gingival Resection Treatment

Treatment of gingival resection with serious atrophy of interdental gingiva and bone tissue between 21st and 22nd teeth — successful regeneration.

Post-Cystotomy Filling

Successful filling of dental defect after cystotomy procedure — demonstrating remodelling and formation of bone tissue with no side effects.

Clinical observations conducted at New-Dent Stomatological Center, Lublin, Poland and Animal Surgery Clinic, University of Life Sciences, Lublin

Scientific Research

Published Research

07 peer-reviewed papers
01

Efficacy of a Novel Adaptable and Moldable Synthetic Polymer, in Open Socket Preservation Without a Membrane: Ease of Use and Volume Preservation in Alveolar Bone RegenerationNEW 2026

Krasny K., Wróblewski S., Wojtowicz A., Kamiński A.

Engineering of Biomaterials (Inżynieria Biomateriałów) 174, 2026 · 2026

02

Behavior of new hydroxyapatite/glucan composite in human serum

Borkowski L., Lubek T., Jojczuk M., Nogalski A., Belcarz A., Palka K., Hajnos M., Ginalska G.

J. Biomed. Mater. Res. Part B, 2018 · 2018

03

Unexpected reaction of new HAp/glucan composite to environmental acidification: Defect or advantage?

Borkowski L., Kiernicka M., Belcarz A., Palka K., Hajnos M., Ginalska G.

Biomed. Mater. Res. B Appl. Biomater. 2017 · 2017

04

The comparison study of bioactivity between composites containing synthetic non-substituted and carbonate-substituted hydroxyapatite

Borkowski L., Sroka-Bartnicka A., et al.

Mater. Sci. Eng. C 2016, 62, 260-267 · 2016

05

Biphasic mode of antibacterial action of aminoglycoside antibiotics-loaded elastic hydroxyapatite-glucan composite

Belcarz A., Zima A., Ginalska G.

Int. J. Pharm. 2013, 454, 285-295 · 2013

06

Application of β-1,3-glucan in production of ceramics-based elastic composite for bone repair

Belcarz A., Ginalska G., Pycka T., et al.

Centr. Eur. J. Biol. 2013, 8, 534-548 · 2013

07

Efficacy of a Novel Adaptable and Moldable Synthetic Polymer, in Open Socket Preservation Without a Membrane (Original)

Krasny K., Wroblewski S., Wojtowicz A., Kaminski A.

Biomaterials · 2021

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