Vision
World-class trauma fixation made accessible without compromise on materials, tolerance or documentation.
Company
Built around precision, traceability and trust
Founded in 1998, Anlon has grown from a specialist turning shop into a vertically integrated orthopedic trauma manufacturer serving distributors and hospitals across regulated markets.
28+
Years of engineering
45+
Export countries
ISO
13485 quality system
Operating Principles
Every implant moves through a controlled chain
The company is structured around three habits: responsible engineering, documented quality and responsive distributor support.
Mission
Design, manufacture and supply implant systems that meet global clinical and regulatory expectations.
Partnership
Distributor support, fast technical response and long-term accountability across every shipped lot.
Infrastructure
Manufacturing built for medical tolerances
From material inspection to final packing, Anlon keeps the critical stages under documented control so each shipment can be traced, audited and supported.
CNC Manufacturing
Multi-axis machining for plates, nails, screws and instruments.
Metrology Lab
CMM, torque checks, profile inspection and batch validation.
Sterile Workflow
UDI-ready packing, IFU control and sterilisation documentation.
Global Dispatch
Lot-controlled export support for tenders and distributor stock.
Quality Policy
Eight checkpoints, one documented release
The same disciplined path applies across plates, nails, screws, instruments and external fixation systems.
- 1
Design Engineering
CAD modelling, FEA validation and surgeon-led design review.
- 2
Material Inspection
Full traceability on ASTM F136 titanium and F138 steel bar stock.
- 3
CNC Machining
Swiss-type multi-axis machining with in-process metrology.
- 4
Surface Finishing
Anodising, passivation and micro-blasting for biocompatibility.
- 5
Quality Testing
CMM dimensional audit, torque and fatigue testing per ASTM.
- 6
Sterilisation
Validated gamma and EO cycles with dosimetric release.
- 7
Packaging
Double barrier sterile packaging with UDI labelling.
- 8
Dispatch
Lot-controlled global logistics to 45+ countries.
Certifications
Approved for regulated work
Quality credentials are treated as operating controls, not display badges. Each one supports the audit trail behind Anlon's manufacturing and export workflow.
ISO 13485:2016
Quality Management for Medical Devices
Certificate MD 712456
CE Certification
European Conformity, Notified Body
Certificate CE 0123
US FDA 510(k)
Cleared for US distribution
Certificate K203114
ISO 9001:2015
Quality Management System
Certificate QM 884201
Patient-first release
Lots are released only after documentation and inspection are complete.
System approach
Implants, screws and instruments are managed as matched surgical systems.
Export readiness
Distributor support includes catalogues, certificates and technical documentation.