XPartsLab manufactures medical device housings, functional parts, validation samples and fixtures. We support prototype validation, small-batch production and inspection-focused delivery for non-sterile custom components.
Get an Instant Quote See What Types Can Be ManufacturedReview dimensions, assembly, function, material constraints and records before manufacturing non-implantable device and laboratory-equipment parts.
Define critical dimensions, datums, tolerances and fits from the complete assembly and intended engineering test.
Match strength, deformation, edge, motion, clamping and sealing risks to the customer's intended verification method.
Evaluate material and finish against customer-defined mechanical, temperature, humidity, cleaning and appearance requirements.
Align the active drawing, material, process, finish, inspection scope and batch identification for each approved build.
Manufacture structural, enclosure, motion, fluid, sensor and fixture components for engineering verification and low-volume builds.
Choose a process by geometry, material, tolerance, finish, cleaning requirements, quantity and validation stage.
Address dimensional, assembly, material, revision and process risks before engineering verification and low-volume builds.
Review datums, tolerances, hole positions, flatness, fits and sealing features against the complete assembly and intended test.
Align the approved revision, material, finish, inspection scope and batch identification before repeat production.
Compare candidate materials and finishes against customer-provided cleaning, exposure, mechanical and appearance requirements.
Confirm the drawing and bill of materials (BOM) revision, acceptance criteria and agreed inspection records for each build.
Compare prototype and production routes by quantity, tolerance, material, finish, inspection, tooling and target schedule.
Move from project files to an agreed process, controlled build and documented delivery.
Review files, process choice, dimensions, materials, revisions, inspection, lead time and confidentiality before placing an order.
Provide a 3D model and, where available, a 2D engineering drawing:
Selection depends on geometry, material, tolerance, finish, cleaning requirements, quantity and engineering stage:
Define requirements from the complete assembly and intended engineering test:
Use one approved build contract for each release:
Provide the intended environment and customer-owned acceptance criteria:
Confirm the active release before manufacturing:
Focus precision and documentation on features that affect the intended test:
Inspection documentation is agreed during quotation and engineering review. Options include:
Typical production estimates are:
Final timing is confirmed in the quote and depends on part complexity, material availability, quantity, tooling, finishes, inspection and post-processing.
A non-disclosure agreement (NDA) can be signed. Confirm file naming, access, project-number, supplier-access and retention requirements before work begins.
Upload your CAD files and add material, quantity, tolerance, finish and delivery requirements. We will review manufacturability and recommend the next step.
