Next-Generation Arthroscopic Instrumentation
High-performance instrumentation for the demanding arthroscopist. European-grade precision, designed for clinical excellence and sustainable healthcare value. Proudly operating from our headquarters in Chicago, USA 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 quality management system is certified to ISO 13485:2016 and aligned with EU Medical Device Regulation requirements for Class IIa and IIb orthopedic devices. Design controls, risk management per ISO 14971, and post-market surveillance are embedded across our arthroscopy portfolio. FDA 510(k) clearance pathways for our core suture anchors and interference screws are actively progressing through pre-submission review.
Manufacturing Excellence
The Engineering Advantage
Manufactured in ISO Class 7 certified cleanrooms using five-axis CNC machining and Swiss-style lathes. We combine European design standards with high-efficiency automation for arthroscopic implants and instruments.
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 and biocomposites validated for biocompatibility and structural integrity. Titanium bar stock and cobalt-chrome alloys arrive with full material certificates and incoming inspection records.
Micro-injection molding creates complex anchor geometries optimized for pull-out resistance and suture passage. Five-axis CNC and Swiss lathe machining refine threads, eyelets, and cannulated profiles to validated tolerances.
Automated optical inspection and validated gamma and EtO sterilization to SAL 10⁻⁶. Packaged and ready for the sterile field with lot traceability on every pouch.
Regional Insights: South America
Recurring themes from practitioner feedback across our South American supply network.
"The surgical flow is smoother. Less clutter in the tray, more efficiency in the OR."
"Consistent fixation and intuitive instrumentation. The material strength speaks for itself."
"The precision molding of these implants is impressive. They fit well and the delivery system is robust."
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 2008.
ArthroGear is dedicated to advancing the field of sports medicine through relentless innovation in titanium and biocomposite implant technology.
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
Produced under ISO 13485-aligned quality systems with CE Mark (MDR) pathways and validated sterile packaging practices.
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?
ArthroGear 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?
ArthroGear 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?
ArthroGear 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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