510(k) · Cleared
ClearedSuglue-10
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
3M Espe AG · EMA Cement, Dental
Cleared on Jun 3, 2011 as substantially equivalent to K100756 (3M Espe AG Dental Products, 2010) and 2 other predicates after a 101-day review. Its family tree reaches back 10 generations to 1993. 8 later devices descend from it.
- Decided
- Jun 3, 2011
- Review
- 101 days
- Class
- Class II
- Product code
- EMA
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 10 generations to K931812 (1993). 32 ancestors in all, the oldest K871636 (1987). 8 later devices descend from it, 3 citing it directly.
- Root · 10 generations backK931812 New Dentine AdhesiveDentsply Intl. · 1993
- 6 generations between
- 3 generations backK032455 Panavia F 2.0Kuraray Medical, Inc. · 2003
- 2 generations backK094007 Unicem3M Espe AG Dental Products · 2010
- 1 generation backK100756 MALTA3M Espe AG Dental Products · 2010
- This deviceK110508 Suglue-103M Espe AG · 2011
- Descendant · cites it directly · 5 of its ownK153231 G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc. · 2016
- Descendant · 2 generations on · 3 of its ownK200798 G-Cem OneGC America, Inc. · 2020
- Descendant · 3 generations on · 0 of its ownK254109 G-Cem UniversalGC America, Inc. · 2026
- Descendant · 3 generations on · 0 of its ownK254063 iCEM Universal PlusKulzer, LLC · 2025
- Descendant · 2 generations on · 0 of its ownK251946 G aenial Universal Injectable IIGC America, Inc. · 2025
Show all 10 generations
- Root · 10 generations backK931812 New Dentine AdhesiveDentsply Intl. · 1993
- 9 generations backK960823 Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
- 8 generations backK962348 Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
- 7 generations backK964525 Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/ActivatorDentsply Intl. · 1997
- 6 generations backK974486 Clearfil Liner Bond 2VKuraray America, Inc. · 1998
- 5 generations backK990040 Clearfil SE BondKuraray Co. · 1999
- 4 generations backK012442 Modification to Clearfil SE BondKuraray Medical, Inc. · 2001
- 3 generations backK032455 Panavia F 2.0Kuraray Medical, Inc. · 2003
- 2 generations backK094007 Unicem3M Espe AG Dental Products · 2010
- 1 generation backK100756 MALTA3M Espe AG Dental Products · 2010
- This deviceK110508 Suglue-103M Espe AG · 2011
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K153231G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc. · 2016 · cites it directly5descendants
- K200798G-Cem OneGC America, Inc. · 2020 · 2 generations on3descendants
- K254109G-Cem UniversalGC America, Inc. · 2026 · 3 generations on0descendants
- K254063iCEM Universal PlusKulzer, LLC · 2025 · 3 generations on0descendants
- K251946G aenial Universal Injectable IIGC America, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K931812 | New Dentine Adhesive | Dentsply Intl. | 1993 | — |
| −9 | K960823 | Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding Agent | Dentsply Intl. | 1996 | — |
| −8 | K962348 | Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding Agent | Dentsply Intl. | 1996 | — |
| −7 | K964525 | Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/Activator | Dentsply Intl. | 1997 | — |
| −6 | K974486 | Clearfil Liner Bond 2V | Kuraray America, Inc. | 1998 | — |
| −5 | K990040 | Clearfil SE Bond | Kuraray Co. | 1999 | — |
| −4 | K012442 | Modification to Clearfil SE Bond | Kuraray Medical, Inc. | 2001 | — |
| −3 | K032455 | Panavia F 2.0 | Kuraray Medical, Inc. | 2003 | — |
| −2 | K094007 | Unicem | 3M Espe AG Dental Products | 2010 | — |
| −1 | K100756 | MALTA | 3M Espe AG Dental Products | 2010 | — |
| 0 (this device) | K110508 | Suglue-10 | 3M Espe AG | 2011 | — |
| +1 | K153231 | G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer | GC America, Inc. | 2016 | — |
| +2 | K200798 | G-Cem One | GC America, Inc. | 2020 | — |
| +3 | K254109 | G-Cem Universal | GC America, Inc. | 2026 | — |
| +3 | K254063 | iCEM Universal Plus | Kulzer, LLC | 2025 | — |
| +2 | K251946 | G aenial Universal Injectable II | GC America, Inc. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1988 | 1 | 0 |
| 1990 | 2 | 0 |
| 1991 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 5 | 0 |
| 1995 | 1 | 0 |
| 1996 | 1 | 0 |
| 1998 | 2 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2002 | 1 | 0 |
| 2006 | 1 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2019 | 2 | 0 |
| 2020 | 1 | 0 |
| 2025 | 3 | 0 |
| 2026 | 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 EMA? 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 EMA device
- #1 K254109 G-Cem Universalscore 15.0 · 13 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K100756 | MALTASummary page 1…ommon Name: ........................................ Adhesive resin cement Predicate Devices Malta by 3M ESPE, Germany ........................ K100756 Panavia F 2.0 by Kuraray Medical Inc., Japan .... K032455 Nexus 3 by Kerr Corporation, U.S.A...............K062519… | 2010 |
| * | K032455 | Panavia F 2.0Summary page 1…resin cement Predicate Devices Malta by 3M ESPE, Germany ........................ K100756 Panavia F 2.0 by Kuraray Medical Inc., Japan .... K032455 Nexus 3 by Kerr Corporation, U.S.A...............K062519… | 2003 |
| * | K062519 | NEXUS 3Summary page 1…any ........................ K100756 Panavia F 2.0 by Kuraray Medical Inc., Japan .... K032455 Nexus 3 by Kerr Corporation, U.S.A...............K062519 OCO7 Descrip~tion for the Prema… | 2006 |
What descends from it? (8)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
- The line of descent spans 18 years and passes through 6 companies; a new generation was cleared every 1.0 years on median.
- 1 of the 32 ancestors has a recall of any class.
- Of its descendants, K153231 (GC America, Inc., 2016) has gone furthest, with 5 descendants of its own.
- 4 other devices also cite its predicate K100756.
How does its category compare?
All EMA devicesEMA Cement, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · EMA
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EMA
106in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EMA
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EMA
9in 2025
MAUDE reports naming product code EMA, 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 | 6 | 48 | 0 | 33 |
| 2008 | 13 | 71 | 2 | 50 |
| 2009 | 10 | 86 | 1 | 90 |
| 2010 | 14 | 86 | 1 | 106 |
| 2011 | 8 | 79 | 5 | 224 |
| 2012 | 10 | 128 | 0 | 249 |
| 2013 | 12 | 178 | 0 | 385 |
| 2014 | 4 | 174 | 0 | 207 |
| 2015 | 9 | 134 | 0 | 85 |
| 2016 | 10 | 182 | 0 | 16 |
| 2017 | 3 | 141 | 0 | 13 |
| 2018 | 3 | 237 | 0 | 4 |
| 2019 | 7 | 127 | 0 | 12 |
| 2020 | 8 | 164 | 0 | 5 |
| 2021 | 4 | 184 | 0 | 8 |
| 2022 | 7 | 245 | 0 | 3 |
| 2023 | 2 | — | 1 | 6 |
| 2024 | 3 | 59 | 0 | 5 |
| 2025 | 10 | 106 | 0 | 9 |
| 2026 | 7 | 150 | 0 | — |
What is it indicated for?
Final cementing of all-ceramic, composite, or metal inlays, onlays, crowns and bridges; 2-3-unit Maryland bridges and 3-unit inlay/onlay bridges (excluded for patients with bruxism or periodontitis)
Final cementing of posts and screws
Final cementation of all-ceramic, or composite veneers
Final cementation of all-ceramic, composite, or metal restorations on implant abutments
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110508 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110508: Suglue-10.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110508
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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