Sports medicine procedures may require tendon replacement, ligament reconstruction, management of a bone tunnel or defect, and a point-of-care autologous preparation within the same service line.
Evologics provides a connected portfolio of tendon allografts, bone graft materials, synthetic scaffolds and BMA/PRP processing systems.
Tendon allografts provide options for selected ligament and tendon reconstruction procedures without requiring harvest of the same tissue from the patient.
Available tissue may include:
Graft selection should account for patient factors, required dimensions, fixation method, tissue processing and rehabilitation strategy.
DBM putties, fibers and other nonstructural forms may be evaluated where a surgeon requires graft material around bone tunnels, osseous voids or associated bony procedures, consistent with the product labeling.
Cancellous tissue, structural configurations and synthetic bone-graft materials provide additional options for procedures involving bone defects, osteotomies or fixation sites.
Point-of-care systems process the patient’s own blood or bone marrow aspirate for clinician-directed use.
Evidence differs substantially between applications, preparation methods and patient populations. The systems should be presented as processing technologies, not as guaranteed treatments for pain, cartilage loss or tendon healing.
The portfolio may be discussed in connection with:
Evologics supports graft selection, specifications, ordering, tissue tracking, facility documentation and product education.
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 current availability or schedule a portfolio review.
