# K152636: Laser Dock

- Pathway: 510(k) (Traditional)
- Applicant: Patient Pocket, LLC
- Decided: Dec 17, 2015 after 93 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K170215: LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock (2017), 0 descendants of its own

## Indications for use
The Laser Dock is designed for use with Ho:YAG, Nd:YAG, CO2 and KTP laser systems when laser fibers are deployed.

Source page: https://510kreport.com/device/K152636
Methodology: https://510kreport.com/methodology