# K223763: ZeptoLink IOL Positioning System

- Pathway: 510(k) (Traditional)
- Applicant: Centricity Vision, Inc.
- Decided: Apr 11, 2023 after 117 days
- Product code: PUL (Apparatus, Cutting, Radiofrequency, Electrosurgical, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K001498 (2000). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210827: ZEPTO Precision Capsulotomy System, Centricity Vision, Inc. (2021) Summary page 4.

## Indications for use
The ZeptoLink IOL Positioning System is indicated for use in performing anterior capsulotomy during cataract surgery.

Source page: https://510kreport.com/device/K223763
Methodology: https://510kreport.com/methodology