Medisplint
Medisplint
As the global incidence of spinal degenerative diseases rises, the clinical demand for advanced, biocompatible implants has reached unprecedented levels. The transition from traditional rigid fusion options to biologically responsive titanium solutions is crucial. Today, medical device procurement managers and spinal surgeons require components that possess superior biomechanical characteristics, promote rapid osseointegration, and reduce the risk of postoperative complications.
Medisplint Orthopedic Instruments Co., Ltd. addresses these demands directly. We specialize in the manufacturing and export of high-grade Titanium Interbody Cages engineered for TLIF, PLIF, ALIF, and LLIF approaches. By leveraging our deep manufacturing knowledge and robust quality systems, we provide medical professionals worldwide with orthopedic devices that deliver stability and long-term fusion success.
Optimized modulus of elasticity to minimize stress shielding and risk of cage subsidence.
Specialized surface modifications that encourage direct bone apposition to the titanium structure.
While PEEK features a modulus of elasticity close to cortical bone, it lacks osteoinductive properties, which can result in fibrous encapsulation. Medical grade Titanium (Ti-6Al-4V ELI) combined with textured surfaces improves structural integration, creating a stable environment for bony fusion.
Additive manufacturing and chemical etching allow us to produce titanium cages with open-pore matrices. This porous architecture mimics trabecular bone, enabling bone ingrowth through the implant rather than simply around it, supporting long-term structural integrity.
Global medical device distributors need partners capable of handling complex logistics and meeting tight deadlines. Medisplint leverages an ecosystem of 1,200 supply chain partners to maintain consistent production and buffer against raw material fluctuations.
Raw Materials
Slitting
CNC Machining
Machining
Milling
Inspection and Packing
Inspection and Packing
Warehouse
Slitting Machine
CNC Machining Center
CNC Milling Machine
Wire Cutting Machine
CNC Lathe
Laser Marking Machine
Design
Lab
Inspection
Inspection
Fatigue Tester
Tensile Tester
Two Dimensional Measuring Instrument
Hardness Tester
Bone Screw Performance Tester
Our OEM titanium interbody cages are designed and manufactured to meet rigorous global regulatory standards, including CE certification and ISO 13485 quality systems. We support clinical and commercial operations across various markets by offering customized product lines and comprehensive regulatory documentation.
Manufactured in compliance with Class III standards to ensure maximum safety and performance in long-term implantations.
Full material traceability from raw titanium bars through CNC machining and sterile packaging to the final implantation step.
Full-service OEM branding, including laser marking and custom packaging solutions, designed to align with regional regulatory requirements.
Medisplint exports orthopedic implants to partners in Europe, Southeast Asia, the Middle East, and South America. We collaborate with hospitals, regional distributors, and medical device suppliers to establish robust and compliant local supply chains.
Developing micro- and nano-textured titanium surfaces to promote earlier bone apposition and reduce recovery times.
Advancing the production of open-pore structures to allow vascularization and bone growth throughout the cage matrix.
Expanding our OEM/ODM design catalog to include modular interbody cages that adapt to patient-specific anatomical requirements.
Exploring hydroxyapatite and other bio-absorbable coatings to accelerate the natural healing and fusion process.
We manufacture our orthopedic implants using medical-grade Titanium Alloy (specifically Ti-6Al-4V ELI in compliance with ASTM F136). This material is selected for its biocompatibility, mechanical strength, corrosion resistance, and favorable modulus of elasticity compared to other structural metals.
With a dedicated team of approximately 85 R&D engineering specialists, we offer full design modification, custom prototyping, and private labeling services. We can customize dimensions, lordotic angles, surface profiles, and insert geometries to align with your specific clinical and brand requirements.
Our facilities and production lines operate under a strict quality management system certified to ISO 13485. Our products comply with European CE regulations for Class III medical devices, ensuring compliance with global healthcare standards.
Our cages undergo mechanical testing, including static and dynamic compression, shear tests (in accordance with ASTM F2077 protocols), and subsidence evaluations (ASTM F2267). This testing validates that the implants can withstand the mechanical loads of the human spine.
