Wholesale Enable Patella knee joint component for knee replacement Suppliers, Factories
Product Description
Product Specifications
| Product Name | Enable Patella |
| Available Sizes |
Φ26 mm
Φ29 mm
Φ32 mm
Φ35 mm
|
| Material | UHMWPE |
| Qualification | ISO13485 / NMPA |
| Package | Sterile Packaging, 1 pcs/package |
| MOQ | 1 Pcs |
| Supply Ability | 1000+ Pieces per Month |
Clinical Indications
Arthritic Conditions
Rheumatoid arthritis, post-traumatic arthritis, osteoarthritis, or degenerative arthritis.
Revision Surgery
Failed osteotomies, unicompartmental replacement, or total knee replacement revisions.
About ZATH Knee Implants
ZATH is an orthopedic implants manufacturer that specializes in knee replacement implants. They offer a comprehensive range of knee implants for patients who require knee replacement surgery, including advanced options for total knee replacement and partial knee replacement.
Enable Patella's knee replacement implants are meticulously designed to mimic the natural movement and stability of the knee joint. By utilizing a selection of high-grade materials—including titanium, cobalt, chrome, and polyethylene—these implants provide optimal strength, structural stability, and long-term durability. Overall, knee joint replacement surgery with an Enable Patella implant helps restore mobility and significantly reduce pain for patients with damaged knee joints.
Surgical Process Overview
The standard surgical procedure for knee joint replacement typically involves the following progressive steps:
Preparation
Before surgery, the patient undergoes medical evaluation and testing to ensure clinical suitability, along with physical therapy consultation to plan rehabilitation.
Anesthesia
The patient receives either general anesthesia or regional anesthesia to numb the lower body effectively during the intervention.
Incision
The surgeon performs a precise incision in the knee to properly access and visualize the joint space.
Removal of Damaged Tissue
Damaged bone and arthritic cartilage tissue are resected and prepared from the knee joint surface.
Implantation
The designated knee implant components are accurately placed into the joint space and firmly secured.
Closing the Incision
The surgical incision is meticulously closed utilizing specialized medical stitches or surgical staples.
Post-Operative Care
The patient is closely monitored in the hospital, receives targeted pain management medication, and initiates early physical therapy to support rehabilitation.
Frequently Asked Questions
The Enable Patella is available in four standard diameters: Φ26 mm, Φ29 mm, Φ32 mm, and Φ35 mm to accommodate varied patient anatomies.
The Enable Patella component is constructed from UHMWPE (Ultra-High-Molecular-Weight Polyethylene). Related knee implant systems utilize titanium, cobalt, chrome, and polyethylene to ensure long-term durability and biomechanical stability.
It is indicated for patients with rheumatoid arthritis, osteoarthritis, post-traumatic arthritis, degenerative arthritis, as well as those with failed osteotomies, unicompartmental replacements, or total knee replacements.
The products meet ISO13485 and NMPA certifications. Each implant is supplied in individual sterile packaging (1 piece per package).
The MOQ is 1 piece, with a stable manufacturing capacity exceeding 1,000 pieces per month.
It is engineered to replicate the natural kinematics and stability of the knee joint, facilitating pain reduction and restoring functional joint mobility after surgery.
