# K954505: EZ Stim

- Pathway: 510(k) (Traditional)
- Applicant: Life-Tech Intl., Inc.
- Decided: Dec 10, 1996 after 439 days
- Product code: KOI (Stimulator, Nerve, Peripheral, Electric)
- Device class: 2
- Regulation: 21 CFR 868.2775
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K102084: Stimpod NMS450 Nerve Stimulator (2010), 6 descendants of its own
- K173526: SENTIO MMG Gen 2 (2018), 2 descendants of its own
- K243636: Neuralytix iD3 System (NTX-9001) (2025), 1 descendant of its own
- K260992: iD3 Nav Decompression Probe (NTX-9005); iD3 Ball Tip Stim Probe (NTX-9006); iD3 Nav Ball Tip Probe (NTX-9007) (2026), 0 descendants of its own
- K213049: STIMPOD NMS450 Nerve Stimulator (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K954505
Methodology: https://510kreport.com/methodology