The Standard in Minimally Invasive Repair
Where precision engineering meets arthroscopic biological healing. European-grade precision, designed for clinical excellence and sustainable healthcare value. Proudly operating from our headquarters in Mexico City, Mexico to serve the global orthopedic community.
Pillars of Trust
We build long-term partnerships through documented excellence in arthroscopic device manufacturing.
A Commitment to Global Compliance
Transparency & Roadmap
We operate under an ISO 13485 quality management system with validated processes for CNC machining, molding, and cleanroom assembly of orthopedic implants. EU MDR classification rules are applied during design input to determine conformity routes for soft-tissue fixation and bone anchor products. FDA premarket notification timelines are tracked against predicate device clearances in sports medicine.
Manufacturing Excellence
The Engineering Advantage
Five-axis CNC platforms and citizen-style Swiss lathes run under ISO Class 7 particulate limits for medical device manufacturing. Surface finishes on PEEK anchors and stainless instrument shafts are optimized for sterilization compatibility and surgical handling.
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
Every step is documented, every component measured, every lot releasable.
We qualify PEEK, bio-absorbable polymer matrices, and implant-grade titanium through vendor quality agreements and incoming inspection protocols. Material traceability codes link every anchor body back to its certified raw stock origin.
Multi-cavity molding tools produce consistent PEEK anchor geometry while five-axis CNC units mill undercuts impossible by turning alone. Swiss lathe cells thread titanium and stainless components in single-setup operations.
Automated optical comparators detect surface defects on PEEK anchors before sterilization processing to sterility assurance level 10⁻⁶. Certificate of sterilization and bioburden reduction data support regulatory release documentation.
Regional Insights: South America
Recurring themes from practitioner feedback across our South American supply network.
"Strong cost-to-quality ratio. The components perform comparably to the premium brands we previously sourced."
"The instrumentation is intuitive and helped streamline our rotator cuff workflow. Good quality at a fair price."
"The biomechanical fixation of these anchors has been stable in our follow-ups."
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 2014.
SeraMedical bridges the gap between precision engineering and biological healing, delivering implants that accelerate natural tissue restoration.
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
ISO-aligned process discipline and CE pathway documentation underpin our implant and instrument part lines.
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?
SeraMedical 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?
SeraMedical 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?
SeraMedical 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.