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Device Verification

February 20, 2026

Device Verification (DV) Manufacturing: Bridging Prototype to Regulatory Submission

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Contract services for the design and development, and manufacturing of active, or non-active, and invasive, or non-invasive medical devices, including both sterile and non-sterile devices.

ISO 13485:2016

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ISO Standard for Medical Devices
Medical Device Contract Manufacturing
Quality Assurance for Medical Devices
Development for Medical Devices

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8779 Cottonwood Ave Suite 105, Santee, CA 92071

+1(619) 415-0103

sales@pathwaymedtech.com

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