Xenocor, Inc. - FDA 510(k) Cleared Devices

Xenocor, Inc. has 5 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Latest FDA clearance: Feb 2026. Active since 2016. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Xenocor, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Peak Regulatory Consulting, LLC as regulatory consultant.