# Xenocor, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 5 (2016–2026): 5 510(k) clearances
- Product codes: GCJ (5)
- 510(k) review time since 2016: median 26 days, against 99 for FDA's reviews in the same codes and years (5 of 5 faster)
- Predicates its devices cite: 7 (4 its own); citations of its devices by later devices: 6 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Olympus Winter & Ibe GmbH: 1 (https://510kreport.com/company/olympus-winter-ibe)

## Firms that cite its devices most
- New View Surgical, Inc.: 1 (https://510kreport.com/company/new-view-surgical)
- Oui Medical, Inc.: 1 (https://510kreport.com/company/oui-medical)

## Its most-cited devices
- K161838: Xenocor Xenoscope Laparoscopic System (2016), cited by 3
- K220872: Saberscope5 Laparoscope (2022), cited by 2
- K193315: Xenocor Articulating Xenoscope Laparoscope (2020), cited by 1

## Recent decisions
- 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)

Source page: https://510kreport.com/company/xenocor