Innovating Soft Tissue Fixation
The clinical standard in advanced arthroscopy. European-grade precision, designed for clinical excellence and sustainable healthcare value. Proudly operating from our headquarters in Bogotá, Colombia to serve the global orthopedic community.
Pillars of Trust
Our pillars unite regulatory discipline, biomechanical rigor, and dedicated orthopedic expertise.
A Commitment to Global Compliance
Transparency & Roadmap
Compliance is not a checkpoint—it is woven through CAPA, management review, and supplier qualification under ISO 13485. EU MDR unique device identification and EUDAMED registration workflows are implemented for traceable implant distribution. FDA Quality System Regulation alignment ensures dual compliance for U.S. and European orthopedic device markets.
Manufacturing Excellence
The Engineering Advantage
ISO Class 7 cleanroom enclosures house our injection molding presses and secondary CNC finishing stations for arthroscopy parts. Swiss turning centers produce cannulated screws and pin guides with documented Cpk values exceeding customer specifications.
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 certified raw stock to sealed implant pouch—a controlled orthopedic journey.
Biocompatibility-tested PEEK, PLDLA, and calcium phosphate composites enter our system with validated supply chain documentation. High-purity titanium for cannulated screws is verified for alloy composition and ultrasonically inspected.
PEEK overmolding and insert-molding techniques combine polymer anchors with titanium or stainless inserts in validated cycles. CNC wire EDM and milling stations cut complex lumens and suture eyelets on finished implant blanks.
Laser micrometry and vision inspection gate every lot before terminal sterilization validated to a 10⁻⁶ SAL. Pouch labeling integrates UDI-DI and production dates for complete traceability to design history files.
Regional Insights: South America
Recurring themes from practitioner feedback across our South American supply network.
"The biocomposite material has worked well in our practice. We are happy with the switch."
"Finally an affordable option that doesn't compromise on anchor strength. The knotless system fits our workflow well."
"Responsive support and useful training materials. The quality is evident from the first use."
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 2019.
MedArthro sets the clinical standard in advanced arthroscopy, combining evidence-based design with rigorous quality manufacturing.
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
Production lots are released against documented criteria under an ISO 13485-oriented quality framework.
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 arthroscopy parts and services do you provide?
MedArthro supplies arthroscopy instruments, suture anchors, interference screws, compatible components, sterile-ready kits, and related clinical support for hospitals, surgeons, and distributors.
What materials are used in your implants?
Our implant lines commonly include medical-grade PEEK and biocomposite options selected for strength, imaging characteristics, and biocompatibility. Material certificates and IFU details are available for qualified accounts.
Are your products manufactured under an ISO 13485 quality system?
MedArthro follows an ISO 13485-aligned quality management approach with documented processes intended to support safety, consistency, and hospital procurement review.
Do you offer surgeon or staff training?
Yes. We provide educational resources and can coordinate training support such as technical overviews, in-service sessions, and evaluation materials for qualified clinical teams.
What is the typical lead time for orders?
Standard orders are typically processed within one business day. International delivery times vary by destination and carrier; account teams can confirm current transit estimates.
Can I request custom instrument sets or kits?
Yes. Modular trays and procedure-oriented kits can often be configured to match surgical preferences. Share your procedure mix and preferred components through the contact form.
How do I become a distributor?
MedArthro works with regional distributors. Use the contact form to inquire about territory interest, expected volume, and partnership requirements.
How are implants sterilized?
Implants are typically supplied sterile-packed using validated Gamma or EtO processes depending on the material and packaging configuration. Instruments follow IFU guidance for compatible reprocessing where applicable.
Do you offer evaluation or demo kits?
Evaluation kits and sterile samples may be available for qualified medical facilities. Contact our team to discuss eligibility and scheduling.
Are PEEK and biocomposite implants MRI-compatible?
PEEK and many biocomposite implants are commonly used when reduced metal artifact is preferred. Always follow the product IFU and your imaging protocol for MRI labeling and conditions.
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
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