Orthopedic procedures require biologic materials with very different jobs. Some provide structural form. Others fill nonstructural bone voids, extend available graft volume, reconstruct tendons or process the patient’s own blood or marrow at the point of care.
Evologics brings these categories together in a portfolio organized around procedure, anatomy and handling requirements.
Evologics DBM is available in multiple handling forms, including putty, crushed matrix, strips, cubes, cortical fibers, fiber boats and blended configurations.
Depending on the specific product labeling, DBM may be evaluated as a nonstructural graft material, graft extender or component of a surgeon-directed grafting strategy.
Cortical and cancellous allografts are available in structural and nonstructural configurations.
Options include structural allograft, tricortical wedges, cervical spacers, foot wedges, cancellous cubes and crushed cancellous tissue.
Synthetic graft materials, including hydroxyapatite and tricalcium-phosphate configurations, provide osteoconductive scaffold options in multiple handling forms.
Selection should reflect the defect, required structure, fixation strategy and controlled labeling.
Tendon allografts support selected ligament and tendon reconstruction procedures.
Portfolio options may include Achilles tendon with bone block, gracilis, semitendinosus and anterior or posterior tibialis tissue.
Point-of-care systems process a patient’s own bone marrow aspirate or blood to create a clinician-directed autologous preparation.
Clinical use, composition and supporting evidence vary by system, preparation protocol and procedure. Product information should not be interpreted as guaranteeing regeneration or a particular outcome.
The portfolio may support discussion around:
Evologics helps teams compare forms, dimensions, handling characteristics, documentation and facility requirements across the orthopedic portfolio.
Product information, specifications, IFUs, evidence and facility needs.
Value-analysis support, regulatory documentation, pricing and product comparison.
Ordering workflow, onboarding, staff education and initial coordination.
Clinical education, representative support, replenishment and follow-up.
Procedure examples are provided for general informational and navigation purposes. They do not establish a product indication, treatment recommendation or expected clinical outcome.
Product selection, preparation, placement and documentation remain the responsibility of the qualified healthcare professional and facility. Use must be consistent with the current Instructions for Use, product labeling, institutional policy and applicable regulatory requirements.
Where website language differs from a controlled product document, the current controlled document governs.
Request orthopedic product information or a facility-specific portfolio review.
