Medical Device Manufacturer · US , Salt Lake City , UT

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

5 submissions · 5 cleared · Since 2016

Total

Cleared

Denied

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.

Regulatory submissions have been managed by University of Utah and Peak Regulatory Consulting, LLC.

Xenocor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Xenocor, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 27, 2026