Industries · Medical
Equipment and instrument components.
We machine components for medical equipment and instrumentation where surface finish, material traceability and cleanliness carry the requirement — with a CMM report in every box.
Scope — read this first
We work on medical equipment, not regulated device manufacture. Neither we nor our manufacturing partner holds ISO 13485.
If your part sits inside a regulated device and your quality system requires a 13485 supplier, we are not that supplier today. That is worth two sentences here rather than a wasted RFQ and a meeting. A great deal of medical-adjacent work sits outside 13485 scope, and that work we are a good fit for.
What we take
Where we are a good fit.
| Family | Typical materials | What usually drives cost |
|---|---|---|
| Instrument housings and enclosures | Aluminium 6061 · stainless 316L | Surface finish and cosmetic consistency |
| Brackets, mounts, structural parts | Aluminium · stainless | Tolerance stack across a mating set |
| Fixtures, jigs and test rigs | Tool steel · aluminium | Repeatability and datum scheme |
| Lab and bench equipment components | Stainless · engineering plastics | Cleanability and chemical compatibility |
| Precision components for sub-assemblies | Stainless · PEEK · PTFE | Concentricity and finish on sealing faces |
Questions
Before you send a drawing.
Are you ISO 13485 certified?
No, and neither is our manufacturing partner. We are telling you that on the page rather than in a meeting because it determines whether we can be in your supply chain at all. If your part sits inside a regulated device and your quality system requires an ISO 13485 supplier, we are not that supplier today — and we would rather say so now than take you through an RFQ first.
So what medical work do you take?
Components for equipment and instrumentation rather than regulated device manufacture: enclosures, brackets, fixtures, jigs, test rigs, bench and lab equipment parts, and precision components where surface finish and cleanliness are the requirement. Plenty of medical-adjacent work sits outside 13485 scope, and that is the work we are a good fit for.
Can you meet a surface finish requirement for cleanability?
Yes. Ra 0.4 µm as standard with verification against drawing callouts, and finer finishes as a quoted secondary operation. Tell us what the surface has to survive — wipe-down, autoclave, a specific agent — because that usually matters more to material choice than the Ra number does.
Do you offer material traceability?
Yes, mill certificates traceable to the heat or lot, issued with the shipment where your drawing calls for it, plus the CMM report that ships with every order.