Engineered for Selective Laser Melting (SLM) and Laser Powder Bed Fusion (LPBF), meeting stringent biocompatibility and mechanical standards.
Ultra-low carbon spherical powder with exceptional corrosion resistance and mechanical toughness for trauma fixation and surgical guides.
View Specifications →
Grade 23 extra-low interstitial alloy and CP-Ti Grade 2/4 powders, ideal for trabecular bone growth and direct dental implant fixtures.
View Specifications →
Open-parameter additive system featuring micron-level spot size, precision atmosphere regulation, and multi-laser productivity for medical parts.
Explore Additive Systems →
One-stop engineering covering structural topology optimization, randomized Voronoi porous scaffolds, and post-HIP metallurgical treatment.
Discover Process Services →The global biomedical implant and dental prosthetics industry is undergoing a paradigm transition from standardized mass production to patient-matched, high-precision customization. Driven by an aging global population, the rising incidence of musculoskeletal trauma, and the rapid expansion of aesthetic dental rehabilitation, the demand for high-performance implantable metals has intensified. Among various metallic biomaterials, medical-grade Stainless Steel and Titanium and its Alloys remain the twin cornerstones of clinical surgery and restorative dentistry, collectively occupying over 80% of the worldwide metallic implant volume.
Historically, orthopedic hardware and dental prostheses were manufactured through traditional subtractive machining (CNC milling), forging, and lost-wax investment casting. While these methods established foundational surgical protocols, they face intrinsic limitations when producing biomimetic porous lattices, undercuts, and thin-walled anatomically conforming structures. The integration of Selective Laser Melting (SLM) and Laser Powder Bed Fusion (LPBF) additive manufacturing technologies has completely redefined implant topology, enabling the direct fabrication of complex trabecular bone structures that accelerate osseointegration and dramatically reduce stress shielding.
Direct printing of complex cellular lattices and personalized anatomical contours without tooling constraints, reducing production cycle times from weeks to hours.
Micro-architected porous titanium mimicking human cancellous bone modulus (1.5–5 GPa), effectively eliminating peri-implant stress shielding.
Fully certified metallurgical purity compliant with ASTM F136, ASTM F138, ISO 5832-1, and ISO 13485 medical device quality systems.
Today's commercial market mandates absolute chemical cleanliness, zero internal porosity in solid struts, and tightly regulated particle size distribution (typically 15–53 μm) for additive manufacturing feedstocks. For surgical device manufacturers and contract manufacturing organizations (CMOs), selecting the optimal alloy between medical stainless steel and titanium is the most critical engineering decision, dictating biomechanical longevity, biological safety, regulatory approval pathways, and total cost of care.
Understanding the fundamental physical, chemical, and biological distinctions between medical stainless steel (chiefly 316L and 316LVM) and titanium alloys (CP-Ti Grade 2/4 and Ti6Al4V ELI Grade 23) is critical for matching materials to clinical indications.
| Property / Characteristic | Medical 316L Stainless Steel (ASTM F138) | Ti6Al4V ELI Grade 23 (ASTM F136) | Commercially Pure Titanium (CP-Ti Gr 4) |
|---|---|---|---|
| Young's Elastic Modulus (GPa) | 190 – 210 (High rigidity) | 110 – 114 (Close to cortical bone) | 100 – 105 (Moderate) |
| Yield Strength (MPa) | 220 – 600 (Cold-worked dependent) | 790 – 860 (High load-bearing) | 480 – 550 (Moderate load) |
| Density (g/cm³) | ~7.95 (Heavier) | ~4.43 (45% lighter than steel) | ~4.51 (Lightweight) |
| Osseointegration Capacity | Low (Forms fibrous tissue encapsulation) | Outstanding (Direct bone-to-implant contact) | Superior (Direct bone bonding) |
| Corrosion Resistance (In Vivo) | Good in passivated state; risk of crevice attack | Exceptional (Stable self-healing TiO₂ oxide film) | Immunity to body fluid attack |
| Primary Clinical Applications | Trauma plates, bone screws, surgical instruments | Spinal cages, hip/knee joints, dental implants | Dental implant fixtures, CMF reconstruction |
Biocompatibility dictates how host tissue responds to an implant over decades. Titanium forms an instantaneous, thermodynamically stable titanium dioxide (TiO₂) passivation layer (2–10 nm thick) when exposed to oxygen. This dielectric layer facilitates direct osteoblast attachment, spreading, and mineralized bone matrix deposition without intermediate fibrous tissue formation—a process termed osseointegration. For permanent dental implants and uncemented orthopedic joints, Titanium is the gold standard.
Conversely, 316L stainless steel relies on a chromium-rich oxide film (Cr₂O₃). While biologically well-tolerated for temporary trauma fixation, long-term exposure to physiological saline containing aggressive chloride ions can cause microscopic pitting or nickel ion leaching in susceptible patients. Consequently, stainless steel is primarily employed for temporary fracture fixation hardware intended for eventual removal, or where fibrous encapsulation is surgically acceptable.
The elastic modulus mismatch between synthetic materials and human cortical bone (~10–30 GPa) is the primary cause of "stress shielding"—a phenomenon where overly rigid metal carries all physical load, depriving adjacent bone of mechanical stimuli and leading to localized bone resorption and aseptic loosening. Stainless steel possesses a high modulus (~200 GPa), making it highly resistant to bending but prone to stress shielding in permanent joint replacements. Titanium alloys boast an inherent modulus nearly half that of steel (~110 GPa). When combined with 3D-printed porous lattice designs (such as diamond, gyroid, or Voronoi architectures), the apparent modulus of titanium can be engineered down to 2–5 GPa, matching trabecular bone and promoting long-term fixation.
Orthopedic surgery demands diverse biomechanical responses depending on anatomical location, mechanical loading conditions, and patient healing timelines. Additive manufacturing and advanced metallurgy have broadened the application envelopes for both metals.
In fracture management, the objective is rapid stabilization followed by bone healing. Stainless steel 316L and 316LVM remain the material of choice for compression bone plates, reconstruction plates, and cortical bone screws due to their exceptional ductility, high shear strength, and cost-effectiveness. Surgeons value stainless steel's tactile feedback during intraoperative contouring, allowing precise bending to bone surfaces without micro-fracturing. For complex peri-articular fractures and pediatric trauma, low-profile Ti6Al4V plates are increasingly utilized due to their high fatigue strength and light weight.
Interbody fusion cages require immediate primary stability, open windows for osteogenic graft placement, and radiological assessability. Additively manufactured Ti6Al4V ELI cages featuring randomized porous trabecular networks have largely superseded traditional smooth PEEK (Polyetheretherketone) implants. The continuous open porosity (60–80% porosity with 300–600 μm pore size) facilitates vascularization and endplate bone bridging. Simultaneously, stainless steel and titanium pedicle screws, rods, and cross-links provide robust multi-level posterior column stabilization.
In total hip arthroplasty (THA), 3D-printed titanium acetabular cups featuring integrated trabecular outer coatings allow direct biological fixation without requiring plasma-sprayed hydroxyapatite (HA) coatings that risk delamination over time. Titanium femoral stems with anatomically tapered geometries provide stable load transfer into the femoral canal. For total knee arthroplasty (TKA), tibial baseplates and femoral components utilize ultra-pure titanium or cobalt-chromium alloys, while specialized intramedullary revision stems utilize medical stainless steel or titanium to restore limb alignment.
Following cranial trauma or oncological bone resection, standard stock implants cannot restore intricate cranial or mandibular anatomy. Utilizing patient CT datasets, custom titanium meshes and mandibular reconstruction bridges are printed on high-precision SLM systems. These custom devices restore facial symmetry, provide rigid fixation for vascularized fibular bone grafts, and reduce operative times by eliminating intraoperative manual plate bending.
In modern restorative dentistry, the intersection of digital intraoral scanning, CAD design, and selective laser melting has transformed laboratory workflows, driving unprecedented fit accuracy and clinical predictability.
Commercially pure Titanium (CP-Ti Grade 4) and cold-worked Ti6Al4V ELI represent the benchmark standard for endosseous dental implants. With micro-textured surface treatments (such as Large-Grit Sandblasting and Acid-Etching / SLA, or anodic oxidation), titanium fixtures achieve accelerated osseointegration, enabling immediate or early functional loading protocols. Custom titanium abutments designed via CAD/CAM provide ideal emergence profiles, supporting soft-tissue peri-implant seal formation and minimizing the risk of peri-implantitis.
Traditionally produced via labor-intensive lost-wax investment casting, RPD frameworks are now directly printed using fine metal powders. Titanium RPD frameworks offer patients unparalleled comfort due to their ultra-light weight (half the weight of traditional cobalt-chromium), taste neutrality, and absence of allergic reactivity. Where high clasp flexibility and low cost are prioritized, specialized medical-grade stainless steel and CoCr formulations provide robust clasp retention without deformation during insertion and removal.
For fully edentulous patients with severe alveolar ridge resorption, custom subperiosteal titanium implants provide an alternative to extensive bone grafting. By mapping the residual bone surface via cone-beam CT (CBCT), a custom-fitted titanium framework is printed with mucosal-penetrating abutments, seating directly onto the cortical bone. Additionally, full-arch hybrid framework bars printed from titanium provide a stiff, passive-fitting foundation for screw-retained zirconia or PMMA prosthetic bridges.
The performance of implantable medical devices fabricated by additive manufacturing is strictly governed by the quality of the starting metal powder and the consistency of the melting process.
For reactive biomaterials like titanium and its alloys, powder must be produced in a crucible-free environment to prevent ceramic inclusion contamination. EIGA (Electrode Induction Melting Gas Atomization) uses an induction coil to melt a slowly rotating high-purity alloy electrode in an inert argon atmosphere, allowing the molten stream to fall directly into a supersonic gas nozzle. This produces spherical, satellite-free powders with low oxygen pick-up, outstanding flowability (Hall flow < 25 s/50g), and high packing density—ideal for defect-free LPBF processing. For stainless steel, Vacuum Induction Gas Atomization (VIGA) provides tight chemical control and low inclusion levels.
As-printed SLM parts exhibit rapid solidification microstructures featuring fine acicular martensite (α' phase) in titanium, which yields high tensile strength but limited ductility. To achieve medical-grade fracture toughness and fatigue resistance, post-processing is mandatory:
Avimetal AM Tech Co., Ltd. (AVIMETAL), established in 2014 as a subsidiary of JCMEH, delivers end-to-end metal powder materials, open-architecture additive systems, and certified processes globally.




Empowering medical OEMs and precision laboratories with integrated powder metallurgy, advanced hardware, and tailored process qualification.
More than a hundred kinds of high-performance metal powder brands, such as titanium alloy, superalloy, aluminum alloy, die steel, and medical cobalt-chromium alloy, are applicable to a variety of metal additive manufacturing processes.
Selective Laser Melting (SLM), Laser Solid Forming (LSF), Laser Cladding (LC), and other open-source additive equipment can help users increase production and efficiency, and achieve batch "smart" manufacturing.
For specific application scenarios, we provide one-stop technical services such as customized material design, powder trial-production, structure optimization, forming technology, heat treatment, surface treatment, detection, and analysis.
Supplying high-purity medical powders and precision 3D printing equipment to hospitals, implant manufacturers, and aerospace leaders worldwide.
Annual production capacity supported by multiple EIGA and VIGA atomization lines with continuous inert gas monitoring.
Annual manufacturing capacity of high-precision industrial and medical metal additive manufacturing printers.

Print the Future
Beauty the World

To Build A World-Class AM Technology Enterprise

Innovation • Integrity
Dedication • Accountability
• Avimetal was founded in Zhongguancun, Beijing, launching the venture of advanced metal powder materials;
• Put the first set of EIGA furnace MT-E50 into production.
• Established Hebei subsidiary;
• Put the first set of VIGA furnace MT-V100 into production;
• Participated in the revision of China's first aerospace standard for metal additive manufacturing.
Explore our complete range of certified metal powders, multi-laser additive manufacturing equipment, and turnkey engineering solutions.
Optimized for high ductility trauma plates, fixation screws, and surgical instruments.
Learn More →
Ultra-clean spherical powder engineered for porous spinal cages and joint arthroplasty.
Learn More →
Unsurpassed biological safety and osseointegration for direct dental implant fixtures.
Learn More →
High-strength, nickel-free alloy for dental crowns, bridges, and partial denture frameworks.
Learn More →
Industrial multi-laser 3D printer for continuous batch production of orthopedic implants.
Learn More →
Compact high-efficiency printer optimized for fast turnaround dental laboratories and clinics.
Learn More →
Parametric design and biomechanical FEA simulation for patient-specific implants.
Learn More →
Comprehensive post-processing, chemical testing, and fatigue validation under ISO 13485.
Learn More →