From engineering review to repeatable production, we manufacture precision dental implant components through controlled processes, documented quality requirements and reliable B2B supply.
From the first technical review to recurring supply, we align engineering, precision machining and quality control around the approved product specification.
Our objective is to help dental laboratories, implant companies and distribution partners receive components that are consistent, traceable and ready for integration into their workflows.
We review product drawings, materials, connection geometry, application requirements and inspection criteria before production begins.
Samples are produced and evaluated to confirm fit, form, manufacturability and alignment with the approved specification.
Defined machining procedures, in-process checks and documented requirements support consistent production for recurring B2B supply.
A structured, review-led process keeps product requirements visible from the initial brief through approved recurring supply.
We align the product type, intended application, drawing, quantity and compatibility requirements.
We confirm materials, dimensions, interface requirements and inspection criteria against the approved specification.
Tooling, work instructions and in-process controls are established for the approved product.
Products are inspected according to defined requirements, with relevant quality records maintained for traceability.
Approved repeat orders are supported through controlled production, inspection and packaging procedures.
Support approved repeat orders with controlled production and packaging.
Our in-house machining capabilities support the complex geometries, connection interfaces and surface requirements found in precision dental implant components.
Combined with engineering review and in-process inspection, five-axis machining allows us to move from prototypes to approved recurring production.
Machining capability for detailed implant component geometries and connection interfaces.
Defined work instructions and in-process checks support repeatability.
Support for prototypes, customized projects and approved recurring orders.
PB Dental’s quality management system is certified to ISO 13485:2016 by SGS.
From material review and process control to final inspection, each stage follows defined and documented requirements designed for medical device production.
SGS Certificate No. CN23/00005933
Valid through 6 November 2026
✓Risk-based quality management
✓Traceable process documentation
✓Validated processes and equipment
✓Continuous improvement
Materials and applicable requirements are reviewed against the approved project specifications.
Defined production steps and in-process controls keep manufacturing requirements visible throughout production.
Inspection results and relevant production records are documented according to project requirements.
Products and required documentation are reviewed before approval for shipment.
Send us your specifications, target quantity and application. Our team will review the project and confirm the next step.
Dental implant components and OEM/ODM solutions for dental laboratories, distributors and industry partners worldwide.
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