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Device Name: OSBONE® DENTAL
lndications for Use:
OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:
- Defects after removal of bone cysts
- Augmentation of the atrophied alveolar ridge
- Sinus lift and sinus floor elevation (subantral augmentation)
- Filling of alveolar defects following tooth extraction for alveolar ridge preservation
- Filling of extraction defects to create an implant bed
- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects
- Support function for a membrane in controlled tissue regeneration (CTR)
- Defects after surgical removal of retained teeth or corrective osteotomies
- Other multi-walled bone defects of the alveolar processes
curasan AG
250-1000µm
In Commercial Distribution
- ECURH05V0250 ()
- Total Volume: 0.5 Centiliter
1 x 0.5 cc
- Synthetic bone graft
Device Name: OSBONE® DENTAL
lndications for Use:
OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:
- Defects after removal of bone cysts
- Augmentation of the atrophied alveolar ridge
- Sinus lift and sinus floor elevation (subantral augmentation)
- Filling of alveolar defects following tooth extraction for alveolar ridge preservation
- Filling of extraction defects to create an implant bed
- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects
- Support function for a membrane in controlled tissue regeneration (CTR)
- Defects after surgical removal of retained teeth or corrective osteotomies
- Other multi-walled bone defects of the alveolar processes
curasan AG
1000-2000µm
In Commercial Distribution
- ECURH05M1000 ()
- ECURH05M10005 ()
- Total Volume: 0.5 Centiliter
5 x 0.5 cc
- Synthetic bone graft
Device Name: OSBONE® DENTAL
lndications for Use:
OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:
- Defects after removal of bone cysts
- Augmentation of the atrophied alveolar ridge
- Sinus lift and sinus floor elevation (subantral augmentation)
- Filling of alveolar defects following tooth extraction for alveolar ridge preservation
- Filling of extraction defects to create an implant bed
- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects
- Support function for a membrane in controlled tissue regeneration (CTR)
- Defects after surgical removal of retained teeth or corrective osteotomies
- Other multi-walled bone defects of the alveolar processes
curasan AG
250-1000µm
In Commercial Distribution
- ECURH05M0250 ()
- ECURH05M02505 ()
- Total Volume: 0.5 Centiliter
5 x 0.5 cc
- Synthetic bone graft
Device Name: CERASORB® Ortho Foam
Mofidication: Mouldable Foam
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x50x4 mm
In Commercial Distribution
- ECURCOM2550 ()
1 x 5.0 cc
- Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam
Mofidication: Mouldable Foam
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x25x2 mm
In Commercial Distribution
- ECURCOM2525 ()
1 x 2.5 cc
- Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam
Mofidication: Mouldable Foam
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x12x4 mm
In Commercial Distribution
- ECURCOM2512 ()
1 x 1.2 cc
- Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam
Mofidication: Flexible Foam Stripe
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
65x65x6 mm
In Commercial Distribution
- ECURCOF6565 ()
1 x 25.0 cc
- Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam
Mofidication: Flexible Foam Stripe
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x50x4 mm
In Commercial Distribution
- ECURCOF2550 ()
1 x 0.5 cc
- Bone matrix implant, composite
Device Name: CERASORB® Ortho Foam
Mofidication: Flexible Foam Stripe
Indication for Use:
Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
curasan AG
25x100x4 mm
In Commercial Distribution
- ECURCOF25100 ()
1 x 10.0 cc
- Bone matrix implant, composite
Device Name: Matriform Strip
Indication for Use:
Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process
curasan AG
100x25x4mm
In Commercial Distribution
- ECUR449100 ()
1 x 10 cc
- Bone matrix implant, composite