# K212762: geko W-2

- Pathway: 510(k) (Traditional)
- Applicant: Firstkind Limited
- Decided: Nov 29, 2021 after 90 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K872976 (1987). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193045: geko™ W-2, Firstkind Limited (2020) Summary page 4.

## Indications for use
The geko W-2 is indicated for: * Increasing local blood circulation * Edema reduction * Increasing microcirculatory blood flow in lower limb soft tissue of patients with venous insufficiency and/or ischemia while the device is active

Source page: https://510kreport.com/device/K212762
Methodology: https://510kreport.com/methodology