510(k) · Cleared
ClearedAdpharma Occlude and Occlude F Dentin Tubule Agent
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Adpharma, Inc. · LBH Varnish, Cavity
Cleared on Oct 2, 2008 as substantially equivalent to K992629 (Centrix, Inc., 1999) after a 72-day review. Its family tree reaches back 1 generation to 1999.
- Decided
- Oct 2, 2008
- Review
- 72 days
- Class
- Class II
- Product code
- LBH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K992629 (1999). No later device cites it as a predicate yet.
- Root · 1 generation backK992629 D/Sense II (Green-or) Dentin DesensitizerCentrix, Inc. · 1999
- This deviceK082071 Adpharma Occlude and Occlude F Dentin Tubule AgentAdpharma, Inc. · 2008
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K992629 | D/Sense II (Green-or) Dentin Desensitizer | Centrix, Inc. | 1999 | — |
| 0 (this device) | K082071 | Adpharma Occlude and Occlude F Dentin Tubule Agent | Adpharma, Inc. | 2008 | — |
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 LBH? 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 LBH device
- #1 K262243 Profisil Freescore 12.9 · 4 generations · 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 |
|---|---|---|---|
| * | K992629 | D/Sense II (Green-or) Dentin DesensitizerSummary page 1…evice) Predicate Device: .................................. Centrix D/SENSE II Dentin Desensitizer 510(k) # K992629 Description of the Device: AdPharmaTM Occlude' Dentin Tubule Agents are for use in one of a number of steps normally… | 1999 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- Its one ancestor has no recall.
How does its category compare?
All LBH devicesLBH Varnish, Cavity: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.
FDA decisions per year · LBH
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LBH
223in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LBH
1in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LBH
7in 2025
MAUDE reports naming product code LBH, 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 | 8 | 69 | 0 | 4 |
| 2008 | 6 | 79 | 0 | 3 |
| 2009 | 4 | 69 | 0 | 5 |
| 2010 | 7 | 107 | 0 | 7 |
| 2011 | 3 | 72 | 0 | 8 |
| 2012 | 4 | 83 | 0 | 7 |
| 2013 | 6 | 160 | 0 | 27 |
| 2014 | 6 | 204 | 3 | 40 |
| 2015 | 2 | — | 0 | 14 |
| 2016 | 2 | — | 0 | 12 |
| 2017 | 0 | — | 0 | 11 |
| 2018 | 0 | — | 2 | 13 |
| 2019 | 2 | — | 1 | 9 |
| 2020 | 5 | 256 | 0 | 10 |
| 2021 | 0 | — | 0 | 15 |
| 2022 | 1 | — | 0 | 7 |
| 2023 | 3 | 167 | 0 | 8 |
| 2024 | 3 | 237 | 0 | 6 |
| 2025 | 4 | 223 | 0 | 7 |
| 2026 | 5 | 64 | 0 | — |
What is it indicated for?
Desensitizing agent for dentin surfaces by occluding dentin tubules to help prevent micro-leakage. Use under direct or indirect restorations following dentin etch and prior to dentin adhesive application. Desensitizing agent for use in treatment of cervical erosion in Class V restorations.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K082071 · printed Nov 4, 2026
Cite this page
510(k) Report. “K082071: Adpharma Occlude and Occlude F Dentin Tubule Agent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K082071
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026