DSI Alyoss is the highest quality allograft bone material. It is a composition of a blend of cortical and cancellous bone and is presented in a convenient, ready-to-use syringe. DSI Alyoss is completely safe and the high quality of the bone is ensured by numerous treatment sequences and exceptional measures. It may be used on its own or mixed with an autogenous bone in order to increase the osteoinductive properties of the graft.

DSI Alyoss is a viable alternative to using an autogenous graft from the patient, bringing a number of significant benefits. No need for a second surgery, along with potential complications and infections, postoperative pain, additional anesthesia, and a longer healing process.

DSI Alyoss is harvested from sections of the ilium and ground into several particulate sizes, resulting in a unique mix. This blend of the cancellous bone’s porous architecture supplies a scaffold, promoting osteoconduction and accelerating revascularization. All of that is done while the cortical element provides a lamellar structure, possessing density and strength similar to that of the patient's own bone.

Only EU-registered tissue banks are used as a source, where virtually all the donors undergo stringent screening and extensive tests before being accepted into the banks. After that, the bone is processed into DBM (Demineralized Bone Matrix) to expose osteoinductive growth factors in highly innovative facilities under an aseptic technique to avoid any possible cross-contamination and to meet strict release standards. The last step of the production is gamma sterilization to deliver a clinically effective product, neutral to the immune reactions of the host.

Indications:

Augmentation or reconstructive treatment of the alveolar ridge.
Filling of bony periodontal defects.
Filling of defects after root resection, apicoectomy, and cystectomy.
Filling of extraction sockets to enhance preservation of the alveolar ridge.
Sinus-lifting.
Filling of periodontal defects in conjunction with products intended for Guided
Tissue Regeneration (GTR).
Guided Bone Regeneration (GBR).
Filling of peri-implant defects

Features:

Convenient handling
Only qualified donors from EU-registered tissue banks after a rigorous screening
Promoting osteoconduction and accelerating revascularization
Similar to that of the patient's own bone
Gamma sterilized
May be used on its own or mixed with an autogenous bone
Cortical and cancellous blend
Excellent clinical results
Top-quality
Safe and reliable
Highly biocompatible
No immunogenic reaction
The rapid growth of the new bone

How to use:

The freeze-dried product should be kept within the set temperature for storing prior to use and each product should be rehydrated individually.
1. Remove double - or triple - wrapping (including outer packaging) and use an aseptic technique to remove the inner packaging to the practitioner with sterile surgical attire to avoid contamination.
2. Check for any damages on the inner packaging.
3. Microbiological culture testing is recommended before the allograft tissue is soaked using a saline solution.
4. Rehydrate the allograft in at basin containing sterilized solution (physiological saline solution, lactic acid, ringer's solution) or any other appropriate antibiotic solution of your preference. The rehydrated allograft should be refrigerated between 1 to 8° C prior to transplantation.
5. Rehydration of the allograft for more than 30 minutes is recommended (Stir the solution using a long sterilized rod for 15 seconds).
6. The product should be cleaned about 3 times by changing the solution to remove any remaining reagents.
7. All preparations should be carried out before transplanting the allograft.

Package:

REF	Content
AG25	0.25cc bone graft in a syringe
AG50	0.50cc bone graft in a syringe
AG100	1.00cc bone graft in a syringe