# K151102: Bausch + Lomb Injector System

- Pathway: 510(k) (Special)
- Applicant: Bausch & Lomb, Inc.
- Decided: May 22, 2015 after 28 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: 7 generations back to K930320 (1994). 11 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131958: Bausch & Lomb Injector System, Bausch & Lomb (2014) Summary page 4.

## Most influential descendants
- K181401: RxSight Insertion Device (2018), 4 descendants of its own
- K192926: RxSight Insertion Device (2020), 3 descendants of its own
- K231466: RxSight Insertion Device (2023), 2 descendants of its own
- K231838: RxSight® Insertion Device (63002) (2023), 1 descendant of its own
- K261174: RxSight® Insertion Device (2026), 0 descendants of its own

## Indications for use
The Bausch + Lomb Injector System is indicated for the folding and insertion of Bausch + Lomb intraocular lenses cleared or approved for use with this IOL Injector system.

Source page: https://510kreport.com/device/K151102
Methodology: https://510kreport.com/methodology