# K133146: Bausch + Lumb, VIS100 Injector System

- Pathway: 510(k) (Special)
- Applicant: Bausch & Lomb
- Decided: Jan 3, 2014 after 78 days
- Product code: MSS (Folders And Injectors, Intraocular Lens (Iol))
- Device class: 1
- Regulation: 21 CFR 886.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K930320 (1994). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113852: Bausch & Lomb Iol Injector, Bausch & Lomb, Inc. (2012) Summary page 1.

## Indications for use
The Bausch + Lomb VIS 100 Injector System is indicated for folding and injection of Bausch + Lomb iuntraocular lenses approved for use with this injector.

Source page: https://510kreport.com/device/K133146
Methodology: https://510kreport.com/methodology