Uncompromising Quality for the OR
Exacting precision for arthroscopic soft tissue repair. European-grade precision, designed for clinical excellence and sustainable healthcare value. Proudly operating from our headquarters in Panama City, Panama to serve the global orthopedic community.
Pillars of Trust
Transparency, precision, and material science form the foundation of our partnership.
A Commitment to Global Compliance
Transparency & Roadmap
Our manufacturing processes are strictly aligned with the EU Medical Device Regulation (MDR) and ISO 13485:2016 standards. We are currently in the advanced stages of the FDA 510(k) submission process for our core arthroscopic portfolio.
Manufacturing Excellence
The Engineering Advantage
Manufactured in ISO Class 7 Certified Cleanrooms using 5-axis CNC machining and Swiss-style lathes. We combine European design standards with high-efficiency automation.
Material Integrity
Biomaterial Innovation
- Titanium: Grade 5 Ti6Al4V ELI
- PEEK: High-grade PEEK-OPTIMA™ polymers
- Bio-absorbables: PLDLA / TCP biphasic compounds
Validated Testing
Evidence-Based Biomechanics
Every implant design undergoes rigorous static & dynamic fatigue testing according to ASTM F543 standards for metallic medical bone screws.
Precision Process
From powder to patient, quality is engineered into every micron.
Sourcing highest-grade PEEK & Biocomposites. Validated for biocompatibility and structural integrity.
Micro-injection molding creating complex geometries. Optimized for rapid osseointegration.
Automated optical inspection and validated Gamma/EtO sterilization to SAL 10⁻⁶. Packaged and ready for the sterile field.
Regional Insights: South America
Why surgeons across Colombia, Brazil, and Argentina are choosing Ligexa for quality and value.
"Patients are recovering well with zero inflammatory response. The biocomposite material is top-tier. Very happy with the switch."
"The biocomposite material is absorbed beautifully over time, leaving clean native tissue. Highly recommend for sports med fellows."
"Finally an affordable option that doesn't compromise on the strength of the anchors. The knotless system is a game changer."
Global Expansion
From proven success across Europe and the Middle East to transforming sports medicine in the Americas.
Advanced Composites
PEEK-OPTIMA™
Polyether ether ketone polymer with elastic modulus mimicking cortical bone for engaging stress-shielding prevention.
Bio-Composite
Proprietary blend of PLDLA & β-TCP designed for validated osteoconductivity and full absorption over 24 months.
Ti-6Al-4V ELI
Premium medical-grade titanium alloy (Grade 23) ensuring maximum fatigue strength for high-load applications.
✓ MRI-Conditional Compatibility
Our Story
Uncompromising dedication since 2022.
Ligexa delivers exacting precision in soft tissue repair, engineering anchors and fixation devices for the most complex arthroscopic cases.
Engineered to Global Standards
Premium materials, micron-level machining, and uncompromising regulatory compliance.
Advanced Biomaterials
Medical-grade Titanium (Grade 23) and PEEK polymers deliver validated biocompatibility and long-term stability for every implant.
Micron-Precision Manufacturing
Using Swiss-type CNC machining, we maintain extreme tolerances (±0.005mm), ensuring flawless integration between implants and surgical instruments.
Verified Mechanical Strength
All anchors and screws undergo rigorous ASTM F543 testing, validating exceptional pull-out strength and torsional resistance under stress.
Global Regulatory Compliance
Manufactured under strict ISO 13485:2016 quality systems, our products carry the CE Mark (MDR) and achieve a pristine SAL 10⁻⁶ sterility assurance level.
Global Vision
The Americas: Our New Clinical Frontier.
US & LATAM Expansion
We are actively establishing regional logistics hubs in the United States and strategic partnerships across Latin America to provide real-time inventory and clinical support.
Clinical Collaboration
Join our clinical advisory board. We collaborate directly with surgeons to refine implant geometry based on the unique operative demands of the American market.
Frequently Asked Questions
Common questions about our technology and partnership process.
What materials are used in your implants?
We primarily use PEEK-OPTIMA™ and proprietary Bio-Composite materials that offer superior strength and biocompatibility, designed to mimic the natural elasticity of bone.
Are your products ISO certified?
Yes, Ligexa operates under an ISO 13485 certified quality management system, ensuring the highest standards of safety and reliability.
Do you offer training for surgeons?
Absolutely. We provide comprehensive training programs, including cadaver labs and virtual surgical simulations, to ensure proficiency with our systems.
What is the typical lead time for orders?
Standard orders are processed within 24 hours. International shipping times vary but typically arrive within 3-5 business days via our logistics partners.
Can I request custom instrument sets?
Yes, we offer modular instrument trays that can be customized to your specific surgical preferences and procedural needs.
How do I become a distributor?
We are actively expanding our global network. Please use the contact form below to inquire about territory availability and partnership requirements.
What sterilization methods are compatible?
Our instruments are compatible with standard autoclave cycles. Implants are provided sterile-packed (Gamma or EtO) depending on the material.
Do you offer demo kits?
Yes, evaluation kits are available for qualified medical facilities. Contact our sales team to schedule a demonstration.
What is your return policy?
We offer a 30-day return policy for unopened, sterile products. Please refer to our Terms of Sale for detailed conditions.
Are these implants MRI safe?
Our PEEK and Bio-Composite implants are MRI-Conditional. Titanium components are also compatible but may cause minor artifacts depending on the sequence.
Seamless Integration
Designed for immediate OR readiness.
Sterile Packaging Solutions
All implants arrive pre-sterilized via validated Gamma or EtO processes, double-blistered for immediate safe transfer to the sterile field without delay.
Universal Instrument Compatibility
Engineered to work flawlessly with standard arthroscopic instrument sets, minimizing the need for proprietary hospital capital investments.
Request a Partnership & Evaluation
Select your professional role to route your inquiry to the correct department.