# K170215: LaserDock, HolmiumDock, CO2Dock,OmniDock, KTPDock

- Pathway: 510(k) (Traditional)
- Applicant: Patient Pocket, LLC
- Decided: Apr 19, 2017 after 85 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
Longest line of descent: 1 generation back to K152636 (2015). 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)
- K152636: Laser Dock, Patient Pocket, LLC (2015) Summary page 4.

## Indications for use
LaserDock is indicated to hold laser fibers and prevent any unwanted laser emissions from escaping LaserDock. The LaserDock is designed for use with Ho:YAG (“HolmiumDock”), Nd:YAG, CO2 (“CO2Dock”, OmniDock”), and KTP (“KTPDock”) laser systems when laser fibers are deployed.

Source page: https://510kreport.com/device/K170215
Methodology: https://510kreport.com/methodology