Medical device wire and cable assemblies built under revision control.

Medical customers rarely ask for something exotic. They ask that the thousandth assembly be indistinguishable from the first, that any change be documented, and that records exist if a question comes up two years later.

That is a process problem, so we solve it with process: documented work instructions, calibrated tooling with crimp validation, inspection against IPC/WHMA-A-620, and 100% electrical test with retained records.

We are an assembly manufacturer, not a wire mill. We purchase the wire and cable your specification calls out — including high-flex and shielded medical constructions — and manufacture finished assemblies that pass your incoming inspection.

If your documentation names specific approved components, we build to those part numbers. Substitutions are proposed in writing and approved by you, never made on the floor.

Articulating arms, carts, handpieces, and cabling that gets flexed thousands of times need stranded constructions and terminations that tolerate motion. Equipment that is wiped down or sterilized needs sealed transitions and jacket materials that survive the chemistry.

We build overmolded and heat-shrink-sealed transitions, apply strain relief where flex concentrates, and follow the handling and packaging requirements your documentation defines.

Early-stage devices change constantly; approved devices must not change at all. Running both in one USA facility means design iterations move fast, and once the design freezes, production follows the same controlled path without a supplier transition.

Send drawings or a BOM any time — uploads are accepted 24/7 and our USA-based Sales team responds during business hours.