Medical CNC Machining Services

Our medical programmes run to ISO 9001 based quality management with documented inspection and traceability. We do not claim ISO 13485 certification here. If your device file requires an ISO 13485 certified supplier, tell us at the enquiry stage and we will confirm whether we can meet that requirement before you invest time in a quotation.

As standard: mill test certificates with heat-number traceability, and dimensional inspection reports covering the drawing's critical features.

On request: certificates of conformity, material standard compliance statements against ASTM or ISO grades, and CMM reports on critical geometry. State any specific standard requirement (for example ISO 5832 for implant alloys) at quotation stage so the correct grade and paperwork can be confirmed before material is ordered.

Yes. We machine implant-grade titanium such as Ti-6Al-4V and Grade 2, medical stainless steels including 316L and 17-4PH, cobalt chrome wear-resistant alloys, and implant-grade PEEK. Each is supplied against a defined material specification with traceability back to the heat number.

Passivation, electropolishing, bead blasting, and polished finishes down to a mirror surface where the drawing calls for it. For implant and instrument work the finish is usually specified together with a cleanability or biocompatibility requirement, so the finishing route and the cleaning process are planned together rather than selected afterwards.

Parts are machined with defined coolant and handling controls, then cleaned through a multi-stage process before packing. Burrs are removed under magnification on fine internal edges. Where a programme requires cleanroom-compatible handling or documented particulate control, specify it at quotation stage so the process and packing method can be built around it.

Yes. Rapid prototyping runs on a 24–72 hour cycle for design verification, material testing, and pre-clinical evaluation. Once the design is fixed, the same datum strategy and inspection plan carry into regulated production from 100 up to 50,000+ units, so validation results stay representative.

Yes. We sign unilateral or mutual NDAs before drawing review, restrict drawing access to project engineering personnel, do not use customer parts for marketing or sample display, and do not retain or reproduce finished parts without written authorisation. For medical customers the design file is the core asset and we treat it accordingly.