# K161673: LacriPro Punctum Plug

- Pathway: 510(k) (Traditional)
- Applicant: Lacrimedics, Inc.
- Decided: Nov 18, 2016 after 155 days
- Product code: LZU (Plug, Punctum)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K021936 (2002). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021936: Moist Punctal Plug System, Moist Medical, Inc. (2002) Summary page 4.

## Indications for use
LacriPro plugs may be used to: - Treat Dry Eye Syndrome - Treat ocular dryness secondary to contact lens use - Enhance the efficacy of topical ocular medications - Prevent complications due to dry eyes after surgery - Treat the Dry Eye component of ocular surface diseases

Source page: https://510kreport.com/device/K161673
Methodology: https://510kreport.com/methodology