510(k) · Cleared
ClearedEverstick
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Stick Tech, Ltd. · EBI Resin, Denture, Relining, Repairing, Rebasing
Cleared on Nov 5, 2001 as substantially equivalent to K003333 (Stick Tech, Ltd., 2001) after a 150-day review. Its family tree reaches back 1 generation to 2001. 10 later devices descend from it.
- Decided
- Nov 5, 2001
- Review
- 150 days
- Class
- Class II
- Product code
- EBI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K003333 (2001). 10 later devices descend from it, 8 citing it directly.
- Root · 1 generation backK003333 STICKStick Tech, Ltd. · 2001
- This deviceK011788 EverstickStick Tech, Ltd. · 2001
- Descendant · cites it directly · 2 of its ownK030072 Everstick PerioStick Tech, Ltd. · 2003
- Descendant · cites it directly · 1 of its ownK030820 Everstick PostStick Tech, Ltd. · 2003
- Descendant · cites it directly · 1 of its ownK021126 Everstick OrthoStick Tech, Ltd. · 2002
- Descendant · cites it directly · 0 of its ownK122348 Quartz Splint System (UD, Woven, Rope, Mesh) Quartz Spint Resin QS…Recherches Techniques Dentaires (R.T.D.) · 2012
- Descendant · cites it directly · 0 of its ownK102207 Fiber ForceSynca Marketing, Inc. · 2010
Showing 5 of 10 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 10 · See all- K030072Everstick PerioStick Tech, Ltd. · 2003 · cites it directly2descendants
- K030820Everstick PostStick Tech, Ltd. · 2003 · cites it directly1descendant
- K021126Everstick OrthoStick Tech, Ltd. · 2002 · cites it directly1descendant
- K122348Quartz Splint System (UD, Woven, Rope, Mesh) Quartz Spint Resin QS FlowRecherches Techniques Dentaires (R.T.D.) · 2012 · cites it directly0descendants
- K102207Fiber ForceSynca Marketing, Inc. · 2010 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K003333 | STICK | Stick Tech, Ltd. | 2001 | — |
| 0 (this device) | K011788 | Everstick | Stick Tech, Ltd. | 2001 | — |
| +1 | K030072 | Everstick Perio | Stick Tech, Ltd. | 2003 | — |
| +1 | K030820 | Everstick Post | Stick Tech, Ltd. | 2003 | — |
| +1 | K021126 | Everstick Ortho | Stick Tech, Ltd. | 2002 | — |
| +1 | K122348 | Quartz Splint System (UD, Woven, Rope, Mesh) Quartz Spint Resin QS Flow | Recherches Techniques Dentaires (R.T.D.) | 2012 | — |
| +1 | K102207 | Fiber Force | Synca Marketing, Inc. | 2010 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2002 | 1 | 0 |
| 2003 | 3 | 0 |
| 2004 | 1 | 0 |
| 2006 | 2 | 0 |
| 2007 | 1 | 0 |
| 2010 | 1 | 0 |
| 2012 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in EBI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new EBI device
- #1 K250617 Apex Flexscore 18.3 · 1 generation · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K003333 | STICKSummary page 2…ed for post-trauma, post-operative, or for orthodontic therapy. F-2 everStick™ is substantially equivalent to fibreStick™, approved under 510(k) number K003333 dated January 4, 2001. Testing which has been performed on everStick™ indicates that the device has the same intended use but s… | 2001 |
What descends from it? (10)
8 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K030072 | Everstick Perio | 2003 | 2 |
| K030820 | Everstick Post | 2003 | 1 |
| K021126 | Everstick Ortho | 2002 | 1 |
| K122348 | Quartz Splint System (UD, Woven, Rope, Mesh) Quartz Spint Resin QS Flow | 2012 | 0 |
| K102207 | Fiber Force | 2010 | 0 |
| K063170 | Tender Fiber | 2007 | 0 |
| K033472 | Tescera U-Bar and Barrels | 2004 | 0 |
| K031070 | Carbon Fiber Bridge, Model 28757 | 2003 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
How does its category compare?
All EBI devicesEBI Resin, Denture, Relining, Repairing, Rebasing: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · EBI
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EBI
79in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EBI
2in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EBI
34in 2025
MAUDE reports naming product code EBI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 10 | 53 | 0 | 7 |
| 2008 | 6 | 124 | 0 | 2 |
| 2009 | 3 | 234 | 0 | 5 |
| 2010 | 4 | 95 | 0 | 4 |
| 2011 | 11 | 113 | 0 | 6 |
| 2012 | 3 | 85 | 0 | 9 |
| 2013 | 5 | 135 | 0 | 5 |
| 2014 | 5 | 102 | 0 | 9 |
| 2015 | 9 | 106 | 0 | 8 |
| 2016 | 7 | 147 | 0 | 9 |
| 2017 | 8 | 196 | 0 | 2 |
| 2018 | 5 | 158 | 2 | 2 |
| 2019 | 4 | 127 | 0 | 10 |
| 2020 | 6 | 283 | 0 | 8 |
| 2021 | 4 | 99 | 0 | 25 |
| 2022 | 11 | 154 | 2 | 2 |
| 2023 | 11 | 96 | 0 | 13 |
| 2024 | 9 | 90 | 0 | 1 |
| 2025 | 11 | 79 | 0 | 34 |
| 2026 | 7 | 87 | 0 | — |
What is it indicated for?
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.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K011788 · printed Nov 6, 2026
Cite this page
510(k) Report. “K011788: Everstick.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K011788
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026