# K233902: Centurion™ Vision System (Active Sentry™) (8065753057)

- Pathway: 510(k) (Special)
- Applicant: Alcon Laboratories, Inc.
- Decided: Jan 10, 2024 after 30 days
- Product code: HQC (Unit, Phacofragmentation)
- Device class: 2
- Regulation: 21 CFR 886.4670
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K933880 (1994). 60 ancestors in all.
No later device cites it as a predicate yet.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161794: CENTURION Vision System (Active SentryTM), Alcon Research, Ltd. (2017) Summary page 5.

## Indications for use
The CenturionTM Vision System (Active SentryTM ) is indicated for emulsification, separation, irrigation, and aspiration of cataracts, residual cortical material and lens epithelial cells, vitreous aspiration and cutting associated with anterior vitrectomy, bipolar coagulation, and intraocular lens injection. The AutoSert-T r IOL Injector Handpiece is intended to deliver qualified AcrySof T M intraocular lenses into the eye following cataract removal. The AutoSert-Tr IOL Injector Handpiece achieves the functionality of injection of intraocular lenses. The AutoSert-T r IOL Injector Handpiece is indicated for use with AcrySof TM lenses SN60WF, SN6AD1, SN6AT3 through SN6AT9, as well as approved AcrySof TM lenses that are specifically indicated for use with this inserter, as indicated in the approved labeling of those lenses.

Source page: https://510kreport.com/device/K233902
Methodology: https://510kreport.com/methodology