Custom metal and plastic components for diagnostic, laboratory and medical equipment—manufactured to your drawings.
GPT Precision provides CNC milling and turning for equipment housings, mounting components, mechanical interfaces and development fixtures. We review critical features, material specifications and inspection requirements to define the manufacturing scope for each project.
From structural parts to development fixtures, the component’s function determines which details need attention. We review your drawings and intended use before confirming the project scope.
Housings & structural components
Machined enclosures, mounting brackets, support plates and alignment components for diagnostic, imaging and laboratory equipment.
Key considerations
Mounting interfaces, mating dimensions, alignment datums, threaded features and visible surfaces.
Fixtures & equipment interfaces
Custom positioning fixtures, part-holding components and mechanical interfaces for equipment development, assembly and testing.
Key considerations
Locating features, repeatable positioning, mating components, access clearances and test conditions.
Prototype & development parts
Custom parts for evaluating component geometry, assembly fit and mechanical function during equipment development.
Key considerations
Evaluation objectives, design revisions, critical dimensions and the production requirements that prototypes need to represent.
From drawing to manufacturing review
Review the features that affect fit and function
Identify assembly, material, surface and documentation requirements early to establish a clearer basis for manufacturing review.
Drawing & machined componentPhotography to follow
Critical dimensions & geometry
Highlight mating surfaces, alignment datums, precision bores, threads, thin walls and other functional features. Provide drawing tolerances and acceptance criteria so manufacturing feasibility and inspection methods can be evaluated together.
Material grade & condition
Common machining materials include TC4 titanium alloy, 316L stainless steel, aluminum alloys and POM. Specify the required grade, condition and applicable material standards. Suitability for the intended application and any special material requirements should be evaluated as part of the project review.
Surface finish & handling
Identify functional surfaces, cosmetic requirements, edge conditions and finishing specifications. Where applicable, include cleanliness, packaging, fluid-contact or sterilization-related requirements for scope review before production.
GPT Precision is ISO 9001:2015 certified. Inspection and documentation requirements are reviewed against your drawings, specifications and agreed acceptance criteria.
Dimensional inspection
Inspection methods can include coordinate measuring machines (CMM), optical measurement, dimensional gauges, inspection fixtures and fit and function gauges. Methods and reporting requirements are reviewed against part geometry, critical characteristics and the agreed inspection scope.
Inspection reports & first articles
Specify characteristics that require recorded results, the report format and any first-article inspection requirements. The availability, format and scope of requested reports are reviewed and confirmed before the order is placed.
Material records & traceability
Identify required material certificates, lot identification, certificates of conformity and other records. Requested documentation and traceability requirements are reviewed before order acceptance, with the available scope confirmed for the project.
Drawing revisions & acceptance
Provide the controlled drawing revision and the intended use of development samples. The responsible device team determines application-specific validation, approval and release requirements.
Frequently asked questions
Can you machine components for medical equipment?
GPT Precision reviews CNC machining enquiries for equipment housings, structural components, mounting parts, mechanical interfaces and development fixtures. Feasibility and supply scope depend on the drawing, material, intended application and project requirements.
Can development prototypes be used in a finished medical device?
Development samples are manufactured for specified evaluation purposes. The responsible device team determines suitability for finished-device use through the relevant validation and approval process.
How should we specify materials and surface treatments?
Provide the material grade, condition, surface finish and applicable specifications. Identify special contact, cleanliness or sterilization-related requirements for manufacturing scope review.
Are inspection reports and material certificates included?
Identify the inspection reports, material certificates and traceability records you need during the inquiry so availability and scope can be confirmed.
How are quotation and production lead times determined?
Quotation timing is assessed after reviewing the inquiry. Production lead time depends on drawings, materials, quantity and the agreed manufacturing scope, and is confirmed during quotation or order review.
Let’s review your project
Share your drawings for manufacturing review
Tell us what the component does, where it fits in your equipment and which requirements matter most. Share your drawings and specifications so we can discuss machining feasibility, inspection needs and project requirements.
If supplier qualification or confidentiality arrangements are required, please raise these before sharing restricted information.