# K132534: Victus Femtosecond Laser Platform

- Pathway: 510(k) (Traditional)
- Applicant: Technolas Perfect Vision GmbH
- Decided: Feb 14, 2014 after 185 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: 14 generations back to K913697 (1991). 71 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 77 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120426: Victus Laser Platform, Technolas Perfect Vision GmbH (2012) Summary page 1.
- K122386: Victus Femtosecond Laser Platform, Technolas Perfect Vision GmbH (2013) Summary page 1.
- K120732: Lenssx Laser System, Alcon Lensx, Inc. (2012) Summary page 1.

## Most influential descendants
- 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
- K171014: VICTUS Femtosecond Laser Platform (2017), 1 descendant of its own
- K200724: VICTUS Femtosecond Laser Platform (2020), 0 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 * The creation of cuts / incisions in the cornea in patients undergoing cataract surgery or other ophthalmic treatment requiring cuts / incisions in the cornea.

Source page: https://510kreport.com/device/K132534
Methodology: https://510kreport.com/methodology