Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Xenocor, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 12, 2026: Saberscope™ Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 12, 2026 | Saberscope™ Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1)K260177 · GCJ | 510(k) clearances |
| Apr 20, 2022 | Saberscope5 LaparoscopeK220872 · GCJ | 510(k) clearances |
| Jan 27, 2020 | Xenocor Articulating Xenoscope LaparoscopeK193315 · GCJ | 510(k) clearances |
| Jun 1, 2017 | Xenocor Xenoscope Laparoscopic SystemK171344 · GCJ | 510(k) clearances |
| Sep 26, 2016 | Xenocor Xenoscope Laparoscopic SystemK161838 · GCJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
