Industries · Medical Instruments
Aluminum parts for medical instruments
Medical instrument housings need clean surfaces, tight tolerances and a traceable build. We make anodized aluminum housings and components to device specifications under ISO 9001, with material certs and inspection on the record.
What medical parts need from aluminum
Clean finish, controlled tolerance and a record you can audit.
An instrument housing is handled, disinfected and opened repeatedly, so the surface and the edges matter. Extruded aluminum with a sealed anodize gives a smooth, non-porous finish that wipes clean and resists corrosion; machined seats hold the board, display and connectors to one tolerance. For medical work the differentiator is the record: material certificates, in-process checks and final inspection that an auditor can read.
We are ISO 9001 certified and run medical programs under the same documentation, traceability and cleanliness discipline that ISO 13485 requires. Foshan's supply chain supports medical-grade anodizing (Type II/III, no colorants, low particulate) and controlled finishing. Where your audit requires the formal ISO 13485 certificate, we scope the controlled process into the quality plan at quoting — tell us the standard and we match it.
Parts we build for instruments
Housings and components, finished for the clinical environment.
Instrument housings
Extruded body with machined openings, sealed anodize for clean surfaces.
See enclosures →Anodized finishes
Type II / III anodize, dyed or natural, sealed for corrosion and wipe-down.
See anodizing →Quality you can audit
Traceability and inspection, documented per order.
For medical programs we treat documentation as part of the part. Material certificates (EN 10204 3.1 where required), in-process checks on the machined datum and finish, and final inspection against your acceptance plan are recorded and shipped with the order. Surface finish, edge break and coating thickness are measured, not assumed. If your device requires a specific regulatory pathway or standard, raise it at quoting so the quality plan is written to match.
Send us
- Device class and applicable standard (ISO 13485, etc.)
- Housing envelope and mating parts
- Finish and cleanability requirements
- Documentation and traceability needs
Questions buyers ask first
Scope and compliance, answered plainly.
Are you ISO 13485 certified?
We are ISO 9001 certified and operate medical programs under ISO 13485-aligned process controls — material certificates (EN 10204 3.1), full traceability, FOD and cleanliness discipline, and medical-grade anodizing from Foshan partners. If your auditor requires the formal ISO 13485 certificate itself, we scope that into the quality plan at quoting rather than assume a certificate we have not been audited against. Raise the standard early so the controls match.
What finish suits a clinical environment?
A sealed anodize (Type II or Type III, dyed or natural) gives a smooth, non-porous surface that wipes clean and resists corrosion — the usual choice for instrument housings. Coating thickness and seal quality are measured and recorded. Tell us the cleanability and chemical-exposure needs and we specify the process.
Can you supply material certs and traceability?
Yes. Material certificates, in-process inspection and final inspection against your plan are part of the shipment. For medical work we record the alloy, finish and machined datum so the part is auditable across the run and across reorders.
Build your medical aluminum parts
Send the device spec and standard — we propose housing, finish and quality plan together.