Wholesale Enable Tibial Insert Knee Joint Prosthesis Pricelist, Exporters

Product Features ● Restore natural kinematics of the human body through imitating anatomical rolling and sliding mechanism. ● Keep stable even under high diffraction level. ● Design for more preservation of bone and soft tissues. ● Optimal morphology matching. ● Minimize abrasion. ● New generation of instrumentation, more simple and precise operation.

Product Description

1. The anterior incisure avoids interference with patella movement.

2. The thinning rear part of the tibial insert increases flexion, reduces implant knock, and avoids dislocation risk during high flexion.

Product Specifications & Sizing Chart

Enable Tibial Insert . PS Tibial Insert PS Enable Tibial Insert . CR Tibial Insert CR 1-2# 9 mm
1-2# 11 mm
1-2# 13 mm
1-2# 15 mm
3-4# 9 mm
3-4# 11 mm
3-4# 13 mm
3-4# 15 mm
5-6# 9 mm
5-6# 11 mm
5-6# 13 mm
5-6# 15 mm
Material UHMWPE
Qualification ISO13485 / NMPA
Package Sterile Packaging 1pcs/package
MOQ 1 Pcs
Supply Ability 1000+ Pieces per Month

Indications

  • Rheumatoid arthritis
  • Post-traumatic arthritis, osteoarthritis, or degenerative arthritis
  • Failed osteotomies, unicompartmental replacement, or total knee replacement

Biomechanical Stability & Design

  • 1. The anterior bevel post avoids patella strike during high flexion.
  • 2. 7˚ Retroversion angle.

Articular Surface Comparison

Flexion 155 degree can be achieved with good surgical technique and functional exercise

Surgical Procedure & Recovery

During knee joint tibial insert surgery, the surgeon will make an incision in the knee and remove the damaged portion of the tibial plateau. The surgeon will then prepare the bone to receive the tibial insert implant. The tibial insert is a plastic spacer that fits between the tibial plateau and the femoral component.
The surgeon will use specialized tools to precisely fit the tibial insert into the tibial plateau. The fit must be precise to ensure the knee joint operates smoothly and there is no excessive friction between the insert and the femoral component.
Once the tibial insert is in place, the surgeon will close the incision and the patient will begin the recovery process. As with femoral component surgery, patients will typically need to participate in physical therapy exercises to help strengthen the knee and promote healing. After a few months of rehabilitation, patients can normally expect the knee to feel much better and have improved functionality. However, it is important to follow any post-operative instructions provided by the surgeon to ensure optimal healing and recovery.

Frequently Asked Questions (FAQ)

Q: What is the function of a tibial insert in total knee arthroplasty?

The tibial insert functions as a durable, low-friction articulating surface between the femoral component and the tibial plateau, replacing damaged cartilage and facilitating smooth knee joint mobility.

Q: What material is the Enable Tibial Insert manufactured from?

The insert is constructed from medical-grade Ultra-High Molecular Weight Polyethylene (UHMWPE), offering exceptional wear resistance, biocompatibility, and long-term structural reliability.

Q: What is the difference between CR and PS tibial inserts?

CR (Cruciate-Retaining) inserts preserve the posterior cruciate ligament (PCL), whereas PS (Posterior-Stabilized) inserts incorporate a stabilizing post designed to replace the function of a sacrificed or compromised PCL.

Q: How does the thinning rear articular surface design benefit high flexion?

The thinning rear part prevents implant contact and knock, effectively expanding the clearance in deep knee bending and minimizing the risk of subluxation or dislocation during high flexion.

Q: What flexion range can patients potentially achieve?

A flexion angle of up to 155 degrees can be attained when the implant is combined with precise surgical technique and disciplined postoperative functional rehabilitation.

Q: What quality and regulatory standards do these implants satisfy?

The implants comply with rigorous international medical standards, carrying ISO13485 and NMPA certifications, and are individually packaged under validated sterile conditions.

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