Prevent adverse reactions
Controls the risk of harmful corrosion products and device degradation in vivo.
Standardized procedure to evaluate galvanic corrosion between dissimilar metals in implantable devices under simulated physiological conditions—supporting device safety, longevity, and regulatory compliance.
The method evaluates the potential for galvanic corrosion when dissimilar metallic components make electrical contact within the body. By simulating physiological conditions, it assesses risks that could compromise structural integrity or biocompatibility of the device.
Controls the risk of harmful corrosion products and device degradation in vivo.
Reduces chances of premature failure due to galvanic interactions.
Reproducible test data to back design decisions and submissions.
Hip and knee replacements with mixed-metal modular junctions.
Systems where different metal alloys contact within the oral environment.
Stents, pacemakers, and other devices with multiple metallic components.
Determines if alloy combinations are prone to galvanic corrosion under simulated physiological exposure.
Informs safer combinations and design improvements for modular interfaces.
Provides reliable, reproducible data to support safety and longevity claims.
Send device drawings, alloy pairs, and target exposure conditions. We’ll confirm the test plan, endpoints, and reporting.