510(k) Report

510(k) · Cleared

Cleared

G-Cem One

K200798510(k) TraditionalCleared Nov 24, 2020243-day reviewClass II21 CFR 872.3275

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

GC America, Inc. · EMA Cement, Dental

Cleared on Nov 24, 2020 as substantially equivalent to K153231 (GC America, Inc., 2016) after a 243-day review. Its family tree reaches back 12 generations to 1993. 3 later devices descend from it.

Decided
Nov 24, 2020
Review
243 days
Class
Class II
Product code
EMA
Recalls
None
Predicates
1

Its longest line of descent runs back 12 generations to K931812 (1993). 61 ancestors in all, the oldest K833757 (1984). 3 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2000: 4 other ancestors1993: 2 other ancestors2007: 1 other ancestor2006: 2 other ancestors1996: 4 other ancestors1985: 1 other ancestor2008: 1 other ancestor2005: 1 other ancestor2002: 2 other ancestors2001: 2 other ancestors1999: 4 other ancestors1995: 2 other ancestors1994: 5 other ancestors1991: 3 other ancestors2004: 1 other ancestor2003: 1 other ancestor1998: 2 other ancestors1997: 2 other ancestors1990: 4 other ancestors1988: 1 other ancestor1992: 1 other ancestor1984: 1 other ancestor1987: 1 other ancestor2025: 2 descendants cleared2026: 1 descendant clearedReference device: K120243 · GAM-200 · GC America, Inc. · 2012K931812 · New Dentine Adhesive · Dentsply Intl. · 1993×2: 2 generations cleared close together, K960823 (1996), K962348 (1996) K964525 · Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/Activator · Dentsply Intl. · 1997K974486 · Clearfil Liner Bond 2V · Kuraray America, Inc. · 1998K990040 · Clearfil SE Bond · Kuraray Co. · 1999K012442 · Modification to Clearfil SE Bond · Kuraray Medical, Inc. · 2001K032455 · Panavia F 2.0 · Kuraray Medical, Inc. · 2003×2: 2 generations cleared close together, K094007 (2010), K100756 (2010) K110508 · Suglue-10 · 3M Espe AG · 2011K153231 · G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer · GC America, Inc. · 201619801990200020102020
  1. Root · 12 generations backK931812 New Dentine AdhesiveDentsply Intl. · 1993
  2. 8 generations between
  3. 3 generations backK100756 MALTA3M Espe AG Dental Products · 2010
  4. 2 generations backK110508 Suglue-103M Espe AG · 2011
  5. 1 generation backK153231 G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc. · 2016
  6. This deviceK200798 G-Cem OneGC America, Inc. · 2020
  7. Descendant · cites it directly · 0 of its ownK254109 G-Cem UniversalGC America, Inc. · 2026
  8. Descendant · cites it directly · 0 of its ownK254063 iCEM Universal PlusKulzer, LLC · 2025
  9. Descendant · cites it directly · 0 of its ownK242366 OverCEM SA Universal; OverCEM SA Translucent; OverCEM SA Opaque…Overfibers S.R.L. · 2025
Show all 12 generations
  1. Root · 12 generations backK931812 New Dentine AdhesiveDentsply Intl. · 1993
  2. 11 generations backK960823 Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
  3. 10 generations backK962348 Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl. · 1996
  4. 9 generations backK964525 Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/ActivatorDentsply Intl. · 1997
  5. 8 generations backK974486 Clearfil Liner Bond 2VKuraray America, Inc. · 1998
  6. 7 generations backK990040 Clearfil SE BondKuraray Co. · 1999
  7. 6 generations backK012442 Modification to Clearfil SE BondKuraray Medical, Inc. · 2001
  8. 5 generations backK032455 Panavia F 2.0Kuraray Medical, Inc. · 2003
  9. 4 generations backK094007 Unicem3M Espe AG Dental Products · 2010
  10. 3 generations backK100756 MALTA3M Espe AG Dental Products · 2010
  11. 2 generations backK110508 Suglue-103M Espe AG · 2011
  12. 1 generation backK153231 G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc. · 2016
  13. This deviceK200798 G-Cem OneGC America, Inc. · 2020

Most influential descendants

Showing 3 of 3 · See all
  • K254109G-Cem UniversalGC America, Inc. · 2026 · cites it directly0descendants
  • K254063iCEM Universal PlusKulzer, LLC · 2025 · cites it directly0descendants
  • K242366OverCEM SA Universal; OverCEM SA Translucent; OverCEM SA Opaque; OverCEM Ti-Abutment…Overfibers S.R.L. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K931812New Dentine AdhesiveDentsply Intl.1993—
−11K960823Prime & Bond 2.0 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl.1996—
−10K962348Prime & Bond 2.1 Multipurpose Dentin/Enamel Bonding AgentDentsply Intl.1996—
−9K964525Prime & Bond 2.1 M.P. Dentin/Enamel Bonding Agent W/ActivatorDentsply Intl.1997—
−8K974486Clearfil Liner Bond 2VKuraray America, Inc.1998—
−7K990040Clearfil SE BondKuraray Co.1999—
−6K012442Modification to Clearfil SE BondKuraray Medical, Inc.2001—
−5K032455Panavia F 2.0Kuraray Medical, Inc.2003—
−4K094007Unicem3M Espe AG Dental Products2010—
−3K100756MALTA3M Espe AG Dental Products2010—
−2K110508Suglue-103M Espe AG2011—
−1K153231G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc.2016—
0 (this device)K200798G-Cem OneGC America, Inc.2020—
+1K254109G-Cem UniversalGC America, Inc.2026—
+1K254063iCEM Universal PlusKulzer, LLC2025—
+1K242366OverCEM SA Universal; OverCEM SA Translucent; OverCEM SA Opaque; OverCEM…Overfibers S.R.L.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
198510
198710
198810
199040
199130
199210
199320
199450
199520
199640
199720
199820
199940
200040
200120
200220
200310
200410
200510
200620
200710
200810
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202520
202610
FIG. 1 — Lineage of K200798, 1993–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K254109 G-Cem Universalscore 15.0 · 13 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K153231G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer
Summary page 4
…Decision Date G-CEM LinkForce GC America K153231 EMA Primary 07/06/2016 Inc. G-CEM LINKACE (GAM-200)…
GC America, Inc.2016—
†K120243GAM-200GC America, Inc.2012—

Also cleared against K153231: 1 other device →

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K254109G-Cem UniversalGC America, Inc.20260
K254063iCEM Universal PlusKulzer, LLC20250
K242366OverCEM SA Universal; OverCEM SA Translucent; OverCEM SA Opaque; OverCEM Ti-Abutment…Overfibers S.R.L.20250

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 27 years and passes through 7 companies; a new generation was cleared every 2.2 years on median.
  • 2 of the 61 ancestors have a recall of any class.
  • Of its descendants, K254109 (GC America, Inc., 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K153231.

How does its category compare?

All EMA devices

EMA Cement, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · EMA

10in 2025

2007: 62008: 132009: 102010: 142011: 82012: 102013: 122014: 42015: 92016: 102017: 32018: 32019: 72020: 82021: 42022: 72023: 22024: 32025: 102026 (partial year): 7
2007high 14 (2010) · low 2 (2023)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EMA

106in 2025

2007: 48 days median2008: 71 days median2009: 86 days median2010: 86 days median2011: 79 days median2012: 128 days median2013: 178 days median2014: 174 days median2015: 134 days median2016: 182 days median2017: 141 days median2018: 237 days median2019: 127 days median2020: 164 days median2021: 184 days median2022: 245 days median2024: 59 days median2025: 106 days median2026 (partial year): 150 days median
2007high 245 (2022) · low 48 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · EMA

1in 2023

2008: 22009: 12010: 12011: 52023: 1
2007high 5 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EMA

9in 2025

2007: 332008: 502009: 902010: 1062011: 2242012: 2492013: 3852014: 2072015: 852016: 162017: 132018: 42019: 122020: 52021: 82022: 32023: 62024: 52025: 9
2007high 385 (2013) · low 3 (2022)2025

MAUDE reports naming product code EMA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007648033
20081371250
20091086190
201014861106
20118795224
2012101280249
2013121780385
201441740207
20159134085
201610182016
20173141013
2018323704
20197127012
2020816405
2021418408
2022724503
20232—16
202435905
20251010609
202671500—

What is it indicated for?

1. Cementation of all types of all ceramic, resin and metal-based inlays, onlays, crowns and bridges.

2. Cementation of metal, ceramic, fiber posts, and cast post and cores.

3. Cementation of all ceramic and composite veneers.

4. Final cementation of crowns and bridges on implant abutments.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200798: G-Cem One.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200798

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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