Zenith Technical Innovations - FDA 510(k) Cleared Devices

Zenith Technical Innovations has 5 FDA 510(k) cleared medical devices. Based in Gurnee, US.

Latest FDA clearance: Jun 2024. Active since 2018. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Zenith Technical Innovations Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.