Xenocor, Inc.
Xenocor, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 12, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260177 | Saberscope Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1) | Feb 12, 2026 |
| K220872 | Saberscope5 Laparoscope | Apr 20, 2022 |
| K193315 | Xenocor Articulating Xenoscope Laparoscope | Jan 27, 2020 |
| K171344 | Xenocor Xenoscope Laparoscopic System | Jun 1, 2017 |
| K161838 | Xenocor Xenoscope Laparoscopic System | Sep 26, 2016 |