SYNERGY - Bone Grafting Material. Vial 4,0 cc Cancelous Bovine Xenograft granules. Small particle size 350-840 micron. Vial 4,0 cc. - # HU2G-840
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Description
Bone grafting Mat. HU2G-840
DESCRIPTION
SYNERGY Bone grafting material, reference HU2G-840, Bone grafting Mat. HU2G-840. A Xenograft / processed Bone substitute used in guided Bone regeneration (GBR), socket preservation, sinus floor augmentation, and ridge augmentation procedures.
The material provides an osteoconductive scaffold that supports new Bone formation across the defect during the integration period.
CLINICAL APPLICATION
Used in regenerative procedures associated with implant dentistry — including extraction-socket preservation prior to delayed placement, ridge augmentation prior to or simultaneous with implant placement, lateral or transcrestal sinus floor elevation, and treatment of peri-implant osseous defects. The choice of granule size (840 µm vs 2000 µm range) is determined by the practitioner based on defect size and morphology.
PLATFORM & COMPATIBILITY
Compatible with conventional GBR workflows. Often paired with a barrier membrane (collagen or Bovine pericardium) and primary closure to optimize regenerative outcomes. Consult the SYNERGY clinical literature and the practitioner's clinical judgement for case-specific protocols.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HU2G-840 |
|---|---|
| Brand | SYNERGY |
| Product family | Bone grafting Material |
| Designation | Bone grafting Mat. HU2G-840 |
| Format | Granular / particulate (per size designation in name) |
| Origin | Processed Xenograft / Bone substitute |
| Indication | GBR, socket preservation, ridge augmentation, sinus elevation |
| Package | 1pk |
| Regulatory | CE marking · ISO 13485 medical-device QMS |
MATERIALS & SURFACE
Manufactured under controlled biological processing conditions designed to preserve the natural collagen structure and mineral matrix of the source tissue. Lot-controlled production with full traceability from raw material origin through final packaging.
Supplied terminally sterilized using validated methods appropriate to the biological substrate.
STERILIZATION & HANDLING
Supplied sterile, single-use, in primary and secondary protective packaging. Do not re-sterilize. Use only if the sterile barrier is intact at the time of opening. Storage at room temperature, away from direct sunlight and moisture; observe the printed expiration date.
Discard unused product after the procedure per local biohazard regulations. Verify lot number and expiration date prior to clinical use.
QUALITY ASSURANCE
Manufactured under ISO 13485 medical-device quality management and supplied with CE marking for the European market. Each lot is documented with origin traceability, processing parameters and sterility validation records.