Data / Medical devices / United States / Xenocor, Inc.
Xenocor, Inc.: FDA-registered device maker in Salt Lake City, UT, United States, 5 510(k) clearances
Xenocor, Inc. is registered with the FDA (registration 3013445147) in Salt Lake City, UT, United States. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013445147
- Address
- 515 S 700 E, Ste 3e, Salt Lake City, UT, United States, 84102
- Owner or operator
- Xenocor, Inc. (10053582)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- December 19, 2016
- Registered through
- 2026
- Brand names listed
- Saberscope, Saberscope, Saberscope Articulating Laparoscope, Saberscope VPU, Saberscope Video Processing Unit, Xenobox, Xenocor® VPU, Xenocor® Video Processing Unit and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Endoscope, Flexible | GCQ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Laparoscope, Gynecologic (And Accessories) | HET | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 12, 2026 | K260177 | Saberscope Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1) | GCJ | Substantially Equivalent | Xenocor, Inc. | accessdata.fda.gov |
| April 20, 2022 | K220872 | Saberscope5 Laparoscope | GCJ | Substantially Equivalent | Xenocor, Inc. | accessdata.fda.gov |
| January 27, 2020 | K193315 | Xenocor Articulating Xenoscope Laparoscope | GCJ | Substantially Equivalent | Xenocor, Inc. | accessdata.fda.gov |
| June 1, 2017 | K171344 | Xenocor Xenoscope Laparoscopic System | GCJ | Substantially Equivalent | Xenocor, Inc. | accessdata.fda.gov |
| September 26, 2016 | K161838 | Xenocor Xenoscope Laparoscopic System | GCJ | Substantially Equivalent | Xenocor, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Endoscope, Flexible
- All makers of Laparoscope, Gynecologic (And Accessories)
Updated February 12, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.