Xenocor, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
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.
FDA 510(k) cleared devices by Xenocor, Inc.
5 devices
Cleared
Feb 12, 2026
Saberscope™ Laparoscope (SAS-A-536L)
General & Plastic Surgery
22d
Cleared
Apr 20, 2022
Saberscope5 Laparoscope
General & Plastic Surgery
26d
Cleared
Jan 27, 2020
Xenocor Articulating Xenoscope Laparoscope
General & Plastic Surgery
59d
Cleared
Jun 01, 2017
Xenocor Xenoscope Laparoscopic System
General & Plastic Surgery
24d
Cleared
Sep 26, 2016
Xenocor Xenoscope Laparoscopic System
General & Plastic Surgery
83d