# K003333: STICK

- Pathway: 510(k) (Traditional)
- Applicant: Stick Tech, Ltd.
- Decided: Jan 4, 2001 after 71 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K011788: Everstick (2001), 10 descendants of its own
- K030072: Everstick Perio (2003), 2 descendants of its own
- K030820: Everstick Post (2003), 1 descendant of its own
- K021126: Everstick Ortho (2002), 1 descendant of its own
- K122348: Quartz Splint System (UD, Woven, Rope, Mesh) Quartz Spint Resin QS Flow (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K003333
Methodology: https://510kreport.com/methodology