# K110427: Femtec Laser System for Capsulotomy

- Pathway: 510(k) (Traditional)
- Applicant: Technolas Perfect Vision GmbH
- Decided: Nov 22, 2011 after 281 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: 10 generations back to K913697 (1991). 50 ancestors in all.
8 later devices descend from it; 2 cite it directly.
0 of 59 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082947: Lensx 550 Laser System, Lensx Lasers, Inc. (2009) Summary page 1.
- K090633: Lensar Laser System, Lensar, Inc. (2010) Summary page 1.

## Most influential descendants
- K120426: Victus Laser Platform (2012), 7 descendants of its own
- 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

## Indications for use
The Femtec Laser System for Capsulotomy is indicated for anterior capsulotomy during cataract surgery.

Source page: https://510kreport.com/device/K110427
Methodology: https://510kreport.com/methodology