# K150633: ULTRA Telescopes

- Pathway: 510(k) (Traditional)
- Applicant: Olympus Winter & Ibe GmbH
- Decided: Apr 29, 2015 after 49 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K923982 (1993). 1 ancestor in all.
9 later devices descend from it; 3 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K923982: Olympus Oes Laparoscopy System, Olympus Corp. (1993) Summary page 6.

## Most influential descendants
- K161838: Xenocor Xenoscope Laparoscopic System (2016), 6 descendants of its own
- K193315: Xenocor Articulating Xenoscope Laparoscope (2020), 3 descendants of its own
- K220872: Saberscope5 Laparoscope (2022), 2 descendants of its own
- K211250: VisionPort System (2021), 1 descendant of its own
- K260177: Saberscope™ Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1) (2026), 0 descendants of its own

## Indications for use
These endoscopes are intended to be used for endoscopy and endoscopic surgery within the thoracic and peritoneal cavities including the female reproductive organs. The device is also indicated for visualization of transanal and transvaginal applications.

Source page: https://510kreport.com/device/K150633
Methodology: https://510kreport.com/methodology