Medical Device Manufacturing Software 

TriStar helps medical device manufacturers use PLM (PTC Windchill / Windchill+) to connect product data, automate workflows, and reduce rework across the entire product lifecycle.

500+ Windchill implementations | 5,000+ customers | Top PTC partner

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Speed Up Development and Strengthen Traceability With Medical Device PLM

Core PLM Capabilities for Medical Device Teams

Stop Version Chaos

Centralize CAD, drawings, BOMs, and docs in one controlled system so teams work from the same released data.

Improve Traceability Across Teams

Link engineering, quality, and manufacturing activity to the product record for cleaner handoffs and clearer history.

Speed Up Change Control

Replace email approvals with PLM workflows, automated routing, and visibility into what’s pending.

Increase Reuse and Reduce Duplicate Parts

Make it easier to find proven designs with tools like geometry-based model search and standardized libraries.

Why PLM Matters in Medical Device Manufacturing

Medical device companies face unique challenges that demand tighter control over product data and manufacturing processes. PLM software delivers the data governance and access controls device manufacturers need to meet regulatory requirements while maintaining operational efficiency. Revision control and released configurations ensure every team works from approved data. Change control workflows (ECO/ECN) replace manual approvals with automated routing, reducing cycle time. Better collaboration across sites and functions keeps engineering, quality, and manufacturing aligned. And built-in reporting provides the real-time visibility needed for internal reviews and audits.

Common Pain Points TriStar Helps Solve

Many medtech companies struggle with siloed data and duplicate files that create confusion and compliance risks. Slow approvals and change bottlenecks delay time to market. Costly rework from outdated parts and documents eats into margins. Poor reuse leads to part proliferation and unnecessary design work. And as companies grow, scaling to cloud or hybrid environments while integrating systems becomes increasingly complex. TriStar’s PLM expertise helps medical device manufacturers overcome these obstacles and build a competitive advantage through smarter manufacturing operations.

Tools That Power Medical Device Product Lifecycles

TriStar helps you get more value from PLM and engineering tools by aligning systems, workflows, and governance to how your teams work.

The central hub for product data and controlled releases. Windchill provides the revision control, lifecycle states, workflow approvals, and BOM/document management that medical device manufacturing demands. Full traceability and document control support regulatory compliance and quality management across your production processes.

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Cloud scalability with reduced infrastructure overhead—without sacrificing governance. Windchill+ supports faster scaling, distributed teams, and provides a modernization path for companies ready to move beyond on-premise solutions.

Doctor using computer Document Management System (DMS), online documentation database process automation to efficiently manage files

PTC Creo+ keeps CAD aligned with controlled part and BOM revisions to reduce downstream confusion. Better CAD-to-BOM alignment means fewer outdated files and cleaner releases throughout the manufacturing process.

Windchill extensions add usability, reporting, navigation, and workflow improvements where standard setups fall short. Fewer manual steps, faster daily work, and better visibility across your enterprise resource planning ecosystem.

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ModelSearch improves reuse by helping teams find similar parts and assemblies quickly. Less duplicate design work means fewer new parts, faster engineering cycles, and better inventory management of raw materials.

Two business partners are discussing information on tablet computer. Collaborate and discuss project on tablet

TriStar helps teams adopt the system correctly and keep it working as needs evolve. Role-based training, ongoing optimization, and support contracts ensure you get lasting value from your PLM investment.

Engineer Doing 3D CAD Model Design On Computer At Office

Why Medical Device Manufacturers Partner With TriStar

TriStar brings deep PTC expertise as one of the largest PTC VARs globally, specializing in Windchill and Creo. With 500+ Windchill implementations and 5,000+ customers, our proven delivery track record speaks for itself. We develop hands-on innovations—tools and extensions that close real workflow gaps, including Wincom, model search, and automation solutions. Our strong partner status means better PTC access, deeper roadmap insight, and more responsive support pathways. And we provide full lifecycle support from strategy through implementation, migration, training, and ongoing optimization. 

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Industries Supported by TriStar Digital Thread Solutions

  • Aerospace & Defense: Supporting regulatory compliance and mission-critical design.
  • Automotive & Transportation: Managing configuration control and product quality for complex assemblies.
  • Manufacturing/Industrial Equipment: Ensuring data integrity and robust PDM systems.
  • Electronics & High Tech: Accelerating product development with digital asset management.
  • Medical Devices: Maintaining strict quality assurance standards.
  • Consumer Goods: Enabling better decision-making for rapid product launches.

Frequently Asked Questions

Medical device software encompasses the tools that support design, quality control, production, and compliance. PLM serves as the backbone—connecting product data across the lifecycle from initial concept through manufacturing and service. It provides the end-to-end traceability and document control that regulatory demands require.

PLM replaces manual email approvals with automated workflows and routing. Stakeholders receive notifications, can review and approve changes in real time, and the system tracks what’s pending. This visibility eliminates bottlenecks and accelerates change cycles.

Windchill maintains complete revision history, links documents to parts and assemblies, and records who changed what and when. This creates the audit trail medical device companies need to demonstrate compliance with industry standards.

Windchill offers full control for on-premise deployments. Windchill+ provides cloud scalability with reduced IT overhead. The right choice depends on your infrastructure strategy, team distribution, and growth plans.

TriStar follows proven migration methodologies that preserve revision history, relationships, and metadata. We map legacy structures to Windchill, validate data integrity, and ensure nothing critical is lost in the transition.

Implementations typically move through discovery, configuration, pilot testing, training, and phased rollout. Timeline varies based on scope, but TriStar’s experience across 500+ implementations means we anticipate challenges before they become problems.

Ready to Improve Your Medical Device Product Lifecycle?

Faster changes. Fewer errors. Cleaner releases. Stronger traceability. TriStar helps medical device manufacturers run a more controlled, efficient product lifecycle from design through quality, manufacturing, and service.