Our advanced Instron mechanical testing system evaluates the strength, flexibility, and durability of medical devices and materials. In situ testing provides real-time data on how devices respond to surgical handling, stresses, and loads in a simulated environment.
Instron testing quantifies tensile, compressive, and cyclic loading properties up to 1 kN under controlled conditions. This ensures devices meet strength requirements for clinical use.
In situ setups replicate surgical handling and implantation site specific stresses, providing realistic performance data. This confirms devices can withstand clinical environments.
Testing protocols can be tailored to unique designs. This customization ensures results are directly applicable to regulatory submissions.
Our methods align with many ISO standards and FDA requirements for mechanical testing. This provides clients with regulator-ready data.
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Devices are mounted in the Instron systems under validated conditions. Proper setup ensures reproducibility.
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Controlled forces are applied to replicate handling or until failure.
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Stress, strain, and failure data are collected in real time. This provides detailed insights into device durability.
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Results are analyzed and compiled into compliance-ready documentation.
Instron mechanical testing ensures devices meet strength and performance requirements before clinical use.
Instron systems measure tensile, compressive, flexural, and fatigue properties. This provides a comprehensive profile of a device’s mechanical performance.
In situ testing replicates “in-eye” or “in-body” conditions, providing more realistic data than lab-only setups. This ensures devices perform reliably in real-world environments.
Yes, Instron tests can be customized to match device geometry, material type, and clinical use scenarios. This flexibility makes it useful across multiple device types.
Invision Biomedical’s Instron testing delivers the real-world data regulators and patients expect.
