# K011788: Everstick

- Pathway: 510(k) (Traditional)
- Applicant: Stick Tech, Ltd.
- Decided: Nov 5, 2001 after 150 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
Longest line of descent: 1 generation back to K003333 (2001). 1 ancestor in all.
10 later devices descend from it; 8 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)
- K003333: STICK, Stick Tech, Ltd. (2001) Summary page 2.

## Most influential descendants
- 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
- K102207: Fiber Force (2010), 0 descendants of its own

## Indications for use
As reinforcement in manufacturing and/or repairing full or partial dentures as well as overdentures and orthodontic appliances. As reinforcement for temporary and/or permanent plastic/composite inlays, onlays and bridges. As reinforcement for customized splints used to immobilize teeth which may be required post-trauma, post-operative, or for orthodontic therapy.

Source page: https://510kreport.com/device/K011788
Methodology: https://510kreport.com/methodology