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MEDTECH · DENTISTRY

Precision dental components

Qualify Swiss manufacturers for implant interfaces, prosthetic components and dental instrument parts defined by your technical dossier.

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Three component families to distinguish

Small dental components can combine fine threads, tapered interfaces, drive features and demanding surfaces. A commercial product name alone does not establish compatibility. OVEL organises sourcing around the approved drawing, interfaces and customer acceptance criteria.

01

Implant and prosthetic components

Implants, abutments and prosthetic components require their exact geometry, material and intended use. Implant–abutment interfaces, contact areas and surface requirements must be identified in the dossier.

02

Screws and connecting elements

A prosthetic screw or miniature threaded element needs a defined thread, seating surface and drive feature. Dimensional inspection does not replace the assembly-level tightening requirements specified for the system.

03

Dental instrument parts

Shafts, sleeves, bodies and transmission elements have distinct requirements for guidance, runout, assembly, cleaning and service life. Acceptance criteria depend on the instrument and its intended operating conditions.

Interfaces, threads and surface condition

The choice between Swiss-type turning, mill-turn machining and secondary operations depends on access, workholding and batch size. Drawings need measurement datums, any taper geometry, positional tolerances and thread inspection requirements.

Specify the grade and condition of titanium, stainless steel or engineering polymer. Surface treatments belong in the process qualification scope. Material or treatment substitutions require customer approval rather than a decision based only on stock availability.

Compatibility and industrial qualification

For a proprietary interface, the manufacturer works from authorised, approved technical data. Similar appearance does not demonstrate compatibility with an implant system. OVEL helps identify references, supply boundaries and the tests requested by the device owner.

Pilot production evaluates repeatability, edges, setup marks and assembly with mating parts. The offer should distinguish workshop operations from specialist treatment, cleaning and packaging performed elsewhere. This makes the delivery scope and responsibility for each step explicit.

Traceability, cleaning and incoming acceptance

The quality dossier may include material certificates, batch identification, reports for critical characteristics and records of specified operations. Cleanliness, packaging and any sterile delivery requirement are separate specifications. Where ISO 13485 is required, the manufacturer’s certification scope is checked against the activities being sourced.

Prepare your manufacturing enquiry

For a useful quotation, provide revision-controlled drawings, a 3D model, interface references, material grades, finishes, prototype and production quantities, quality requirements and packaging. OVEL coordinates selection and technical exchanges. Manufacturers confirm their capabilities; the device owner remains responsible for validating the device and its interfaces.

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Technical questions

Is an implant trade name enough to obtain a quotation?

A commercial name does not replace an approved drawing. Geometry, interfaces, material, treatment and acceptance criteria are needed for comparable offers.

Can turning and surface treatments form one enquiry?

Yes. Define the scope of each operation, the providers involved and the documents delivered with the final batch.

How should a screw tightening requirement be handled?

Separate the screw’s dimensional requirements from performance in the assembly. The device owner defines the test conditions and acceptance criteria.

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