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Custom molded parts · Made to your design

Custom Injection-Molded Medical Device Enclosures

Build the enclosure around your instrument, its interfaces and its approval requirements.

FECISION reviews custom plastic covers, bases and bezels for non-implantable equipment. Send the controlled part and assembly drawings so that material, tooling, finish and inspection can be quoted together. These are made-to-design components, not stock housings or complete medical devices.

Empty molded medical-equipment upper housing, base and display bezel design examples
Medical Device Enclosures · Product design illustrations

Application fit

External molded components for non-implantable equipment

The intended use and supply boundary determine what must be designed, molded, finished and verified.

Upper housing with a blank display beside a separate base, internal frame and access panel
Assembly interfacesProduct design illustration: include counterpart revisions in the enclosure review.

Tabletop instrument covers

Upper shells and bases with controlled display openings, external appearance and internal equipment clearance.

Display bezels and front panels

Molded interfaces around customer-defined screens and controls, with separately specified seating and cosmetic requirements.

Equipment control housings

Custom component enclosures where fastening, service access and exposure are defined by the equipment team.

Quote-ready inputs

What to send for a meaningful quotation

Use the same drawing and requirements for every proposal. Mark open decisions explicitly so that a low price does not conceal a different deliverable.

Project-specific inputs and review boundaries
AreaPlease provideReview before release
Part and interfacesCAD, controlled drawing, display and lower-housing revisions.Define loose-part datums, assembled gaps, critical surfaces and permitted DFM changes.
Material and exposureExact resin and color if selected, contact conditions and cleaning routine.Review current grade evidence; define part-level compatibility work and substitution controls.
AppearanceCosmetic zones, color reference, texture and inspection conditions.Agree molded limit samples and measurement methods before production approval.
Secondary operationsCoating, masking, printing, inserts and assembly requirements.Keep component tests separate from the complete equipment qualification.
Quality and supplyTrial quantity, repeat demand, traceability and required reports.Define sample release, change notifications, handling and protective packaging.

From drawing to approval

Approve the molded configuration and its evidence

White instrument housing in a locating nest beside a stationary height probe
Defined sample inspectionProduct design illustration: connect sample identity, datums and the measurement method.
  1. Define the supplied component

    Confirm the intended application, controlled interfaces, partner operations and equipment-level responsibilities.

  2. Resolve resin, DFM and finish

    Review wall distribution, display references, gate witnesses, material identity and any surface preparation.

  3. Inspect and assemble samples

    Connect dimensional, cosmetic and coating records to the agreed specimens and counterpart revisions.

  4. Release controlled repeat supply

    Record accepted requirements, open validation items, material changes and packaging controls.

Practical engineering and buying guides

Decisions to make before production

Before you request a quote

Do you supply complete medical devices?

This service is for custom molded enclosure components. Electronics, device assembly and finished-device qualification are separate responsibilities unless explicitly included in an agreed scope.

Which resin should a medical housing use?

There is no universal grade. Intended contact, cleaning exposure, load, appearance and documentation requirements guide a grade-specific review.

Can internal conductive coating be included?

It can be reviewed as a secondary operation. Define the substrate, preparation, coating system, masking and tests. Coating resistance alone is not whole-device EMC approval.

Does non-implantable mean no validation is needed?

No. The equipment manufacturer must define the actual contact, exposure and applicable requirements. Component evidence must match its intended use.

What is required before a firm quote?

Send the component and counterpart drawings, material and finish requirements, trial and production quantities, acceptance package and required timeline. Feasibility and scope are confirmed after review.

Your next step

Discuss the part with its intended function.

Send the enclosure with its mating parts and intended use. We can review a defined molding, finish and sample-approval scope for your custom component.

Explore our injection molding service or review other custom molded applications.

Request A Quote

Tell Us About Your Project

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