# K120426: Victus Laser Platform

- Pathway: 510(k) (Traditional)
- Applicant: Technolas Perfect Vision GmbH
- Decided: Jul 31, 2012 after 169 days
- Product code: OOE (Ophthalmic Femtosecond Laser)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K913697 (1991). 65 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 73 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033354: Femtec Laser Microkeratome, 20/10 Perfect Vision Optische Gerate GmbH (2004) Summary page 1.
- K110427: Femtec Laser System for Capsulotomy, Technolas Perfect Vision GmbH (2011) Summary page 2.
- K113151: Ifs Laser System, Abbott Medical Optics, Inc. (2012). Cleared while this submission was under review Summary page 1.
- K040204: Zyoptix XP Microkeratome, Bausch & Lomb, Inc. (2004) Summary page 1.

## Most influential descendants
- K122386: Victus Femtosecond Laser Platform (2013), 6 descendants of its own
- K132534: Victus Femtosecond Laser Platform (2014), 5 descendants of its own
- K141379: Victus Femtosecond Laser Platform (2015), 3 descendants of its own
- K140615: Victus Femtosecond Laser Platform (2014), 3 descendants of its own
- K151161: VICTUS Femtosecond Laser Platform (2015), 2 descendants of its own

## Indications for use
The VICTUS Femtosecond Laser Platform is indicated for use for: the creation of a corneal flap in patients undergoing LASIK surgery or other treatment requiring initial lamellar resection of the cornea. for anterior capsulotomy during cataract surgery.

Source page: https://510kreport.com/device/K120426
Methodology: https://510kreport.com/methodology