Clinical Confidence in Every Procedure
Streamlined surgical delivery for uncompromised OR efficiency. European-grade precision, designed for clinical excellence and sustainable healthcare value. Proudly operating from our headquarters in Rio de Janeiro, Brazil to serve the global orthopedic community.
Pillars of Trust
Device reliability in arthroscopy starts with science-backed materials and ends with verified release.
A Commitment to Global Compliance
Transparency & Roadmap
Supplier quality agreements enforce ISO 13485 and ISO 10993 material compliance for PEEK pellets, titanium bar stock, and suture materials. EU MDR importers and authorized representatives are qualified for each distribution territory in sports medicine. FDA 510(k) summary and statement documents communicate substantial equivalence for arthroscopic implant families.
Manufacturing Excellence
The Engineering Advantage
We deploy Swiss lathe gang tooling and palletized CNC cells within ISO Class 7 enclosures to maximize throughput for anchor families. Every process is validated for repeatability across shift changes and material lot transitions.
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
Incoming inspection to final release—no shortcuts, no exceptions.
We receive medical-grade PEEK rods, injection-molding-grade biocomposites, and titanium bar with mill test reports and REACH compliance data. Quarantine holds prevent unverified stock from entering cleanroom manufacturing areas.
PEEK implant bodies are molded to near-net shape, then CNC finished for critical bearing and suture contact surfaces. Swiss lathe production runs deliver thousands of titanium anchor shafts per shift with SPC monitoring.
Dimensional CMM reports and visual inspection logs must clear quality review before sterilization loads are processed to SAL 10⁻⁶. Double packaging and desiccant insertion protect PEEK and biocomposite implants through validated shelf life.
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."
"The resorbable material profile fits our sports medicine cases well. A dependable option."
"Simple, effective, and reliable. The PEEK material holds up well under tension in our shoulder cases."
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 2021.
ArthroKit streamlines surgical delivery with pre-configured, sterile-ready kits designed for maximum OR efficiency and zero compromise.
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
Sterility assurance practices and labeled shelf-life controls are part of our standard release workflow.
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?
ArthroKit 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?
ArthroKit 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?
ArthroKit 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
Select your professional role to route your inquiry to the correct department.