Industrial X-Ray CT System

LK Metrology, Derby, UK, has introduced a production-ready computed tomography inspection system optimized for shop-floor deployment. The industrial CT platform combines high-resolution x-ray scanning with advanced reconstruction algorithms to generate detailed volumetric data for internal dimensional measurement and defect detection. Automated analysis tools support GD&T evaluation, porosity assessment, and wall-thickness mapping, enabling nondestructive inspection of molded, machined, and additively manufactured medical components without sectioning or fixturing changes.

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Interferometric Measurement System

A high-precision interferometric measurement system from Micro-Epsilon, Raleigh, NC, has been introduced for nanometer-scale displacement and thickness monitoring in controlled environments. The IMS5200-TH delivers subnanometer resolution with integrated thermal stabilization to minimize drift influctuating production settings. High-speed signal processing enables dynamic measurement of vibration, flatness, and position in real time. Compact sensor heads and fiber-coupled design facilitate integration into semiconductor tools and medical device manufacturing systems requiring noncontact metrology.

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Process Monitoring and Automation Platform

Kistler, Winterthur, Switzerland, has expanded its in-line process monitoring capabilities for regulated manufacturing environments. The maXYmos system integrates force, torque, pressure, and displacement sensors with real-time curve evaluation to verify each assembly step against defined tolerances. Configurable data logging and industrial fieldbus connectivity support closed-loop automation and full traceability. The platform is designed for medical device production lines requiring validated joining, press-fit, and functional test processes with documented quality assurance.

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IVDR Certification

An IVDR-focused certification support program from DNV, Seoul, Korea, has been introduced to assist developers of AI-driven diagnostic systems navigating European regulatory requirements. The service provides structured conformity assessments, review of technical documentation, and evaluation of quality management systems aligned with In Vitro Diagnostic Regulation standards. Specialized expertise in software lifecycle validation, risk management, and clinical performance documentation helps streamline compliance for algorithm-based diagnostic tools seeking CE marking under evolving regulatory scrutiny.

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Medical Design Briefs Magazine

This article first appeared in the April, 2026 issue of Medical Design Briefs Magazine (Vol. 16 No. 4).

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