510(k) · Cleared
ClearedMagicore System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Innobiosurg Co., Ltd. · DZE Implant, Endosseous, Root-Form
Cleared on Oct 15, 2021 as substantially equivalent to K201981 (Innobiosurg Co., Ltd., 2020) and 5 other predicates after a 66-day review. Its family tree reaches back 17 generations to 1990. 1 later device descends from it.
- Decided
- Oct 15, 2021
- Review
- 66 days
- Class
- Class II
- Product code
- DZE
- Recalls
- None
- Predicates
- 6
Its longest line of descent runs back 17 generations to K894595 (1990). 158 ancestors in all, the oldest K874590 (1988). 1 later device descends from it, 1 citing it directly.
- Root · 17 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 13 generations between
- 3 generations backK162099 IBS Implant System IIInnobiosurg Co., Ltd. · 2017
- 2 generations backK173120 CCM Abutment SystemInnobiosurg Co., Ltd. · 2018
- 1 generation backK202418 Magic UCLA Abutment SystemInnobiosurg Co., Ltd. · 2020
- This deviceK212517 Magicore SystemInnobiosurg Co., Ltd. · 2021
- Descendant · cites it directly · 0 of its ownK220517 IBS SystemInnobiosurg Co., Ltd. · 2022
Show all 17 generations
- Root · 17 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 16 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 15 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
- 14 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
- 13 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
- 12 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
- 11 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
- 10 generations backK080744 HG II Fixture SystemOsstem Implant Co., Ltd. · 2008
- 9 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
- 8 generations backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
- 7 generations backK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
- 6 generations backK121585 TS Implant SystemOsstem Implant Co., Ltd. · 2013
- 5 generations backK140507 Hiossen Prosthetic SystemOsstem Implant Co., Ltd. · 2014
- 4 generations backK153350 IBS Implant SystemInnobiosurg Co., Ltd. · 2016
- 3 generations backK162099 IBS Implant System IIInnobiosurg Co., Ltd. · 2017
- 2 generations backK173120 CCM Abutment SystemInnobiosurg Co., Ltd. · 2018
- 1 generation backK202418 Magic UCLA Abutment SystemInnobiosurg Co., Ltd. · 2020
- This deviceK212517 Magicore SystemInnobiosurg Co., Ltd. · 2021
Most influential descendants
Showing 1 of 1 · See all- K220517IBS SystemInnobiosurg Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −17 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −16 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −15 | K993595 | Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon… | Nobel Biocare Uas, Inc. | 2000 | — |
| −14 | K011879 | 3A Dental Implant System | Osseco Biosource, Ltd. | 2002 | — |
| −13 | K051576 | Avana Dental Implant System | Osstem Co., Ltd. | 2005 | — |
| −12 | K062051 | SS System | Osstem Implant Co., Ltd. | 2006 | — |
| −11 | K063861 | GS System | Osstem Implant Co., Ltd. | 2007 | — |
| −10 | K080744 | HG II Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −9 | K082213 | GS Iii Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −8 | K093352 | HG Iii Fixture System | Hiossen, Inc. | 2009 | — |
| −7 | K101096 | HT Iii SA Fixture System | Hiossen, Inc. | 2010 | — |
| −6 | K121585 | TS Implant System | Osstem Implant Co., Ltd. | 2013 | — |
| −5 | K140507 | Hiossen Prosthetic System | Osstem Implant Co., Ltd. | 2014 | — |
| −4 | K153350 | IBS Implant System | Innobiosurg Co., Ltd. | 2016 | — |
| −3 | K162099 | IBS Implant System II | Innobiosurg Co., Ltd. | 2017 | — |
| −2 | K173120 | CCM Abutment System | Innobiosurg Co., Ltd. | 2018 | — |
| −1 | K202418 | Magic UCLA Abutment System | Innobiosurg Co., Ltd. | 2020 | — |
| 0 (this device) | K212517 | Magicore System | Innobiosurg Co., Ltd. | 2021 | — |
| +1 | K220517 | IBS System | Innobiosurg Co., Ltd. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1988 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 2 | 0 |
| 1991 | 1 | 0 |
| 1992 | 1 | 0 |
| 1993 | 11 | 0 |
| 1994 | 6 | 0 |
| 1995 | 7 | 0 |
| 1996 | 11 | 0 |
| 1997 | 6 | 0 |
| 1998 | 4 | 0 |
| 1999 | 7 | 0 |
| 2000 | 5 | 0 |
| 2001 | 9 | 0 |
| 2002 | 12 | 0 |
| 2003 | 4 | 0 |
| 2004 | 6 | 0 |
| 2005 | 3 | 0 |
| 2006 | 8 | 0 |
| 2007 | 7 | 0 |
| 2008 | 9 | 0 |
| 2009 | 2 | 0 |
| 2010 | 4 | 0 |
| 2011 | 2 | 0 |
| 2012 | 3 | 0 |
| 2013 | 1 | 0 |
| 2015 | 3 | 0 |
| 2016 | 2 | 0 |
| 2020 | 3 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 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 DZE? 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 DZE device
- #1 K211090 ZENEX Implant Systemscore 25.4 · 15 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (6)
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 |
|---|---|---|---|
| * | K201981 | Magicore SystemSummary page 4…Number: 872.3640 • Date prepared: 10/14/2021 Predicate Devices: The subject device is substantially equivalent to the following Reference Devices: Primary Predicate K201981, Magicore System manufactured by InnoBioSurg Co., Ltd. Reference Device K153639, OneQ-SL s-Clean Implant System manufactured by… | 2020 |
| * | K153639 | OneQ-SL s-Clean Implant SystemSummary page 4…evice is substantially equivalent to the following Reference Devices: Primary Predicate K201981, Magicore System manufactured by InnoBioSurg Co., Ltd. Reference Device K153639, OneQ-SL s-Clean Implant System manufactured by Dentis Co., Ltd. K192197, Magicore II System manufactured by InnoBioSurg Co., Ltd… | 2016 |
| * | K192197 | Magicore II SystemSummary page 4…imary Predicate K201981, Magicore System manufactured by InnoBioSurg Co., Ltd. Reference Device K153639, OneQ-SL s-Clean Implant System manufactured by Dentis Co., Ltd. K192197, Magicore II System manufactured by InnoBioSurg Co., Ltd. K201621, Magicore II System manufactured by InnoBioSurg Co., Ltd. K2024… | 2020 |
| * | K201621 | Magicore II SystemSummary page 4…rg Co., Ltd. Reference Device K153639, OneQ-SL s-Clean Implant System manufactured by Dentis Co., Ltd. K192197, Magicore II System manufactured by InnoBioSurg Co., Ltd. K201621, Magicore II System manufactured by InnoBioSurg Co., Ltd. K202418, Magic UCLA Abutment System manufactured by InnoBioSurg Co., Lt… | 2020 |
| * | K202418 | Magic UCLA Abutment SystemSummary page 4…stem manufactured by Dentis Co., Ltd. K192197, Magicore II System manufactured by InnoBioSurg Co., Ltd. K201621, Magicore II System manufactured by InnoBioSurg Co., Ltd. K202418, Magic UCLA Abutment System manufactured by InnoBioSurg Co., Ltd. Indications for Use The Magicore System is intended to replac… | 2020 |
| * | K173120 | CCM Abutment SystemSummary page 7…- K212517 Page 4 of 13 (Cleared in K173120) 5.4, 6.4, 7.4, 8.4, 9.4 (Ne… | 2018 |
| † | K162099 | IBS Implant System II | 2017 |
| † | K152520 | Magicore System | 2016 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K220517 | IBS System | 2022 | 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?
- The line of descent spans 31 years and passes through 8 companies; a new generation was cleared every 1.1 years on median.
- 13 of the 158 ancestors have a recall of any class.
- Of its descendants, K220517 (Innobiosurg Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.
- 1 other device also cites its predicate K201981.
How does its category compare?
All DZE devicesDZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · DZE
31in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DZE
184in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DZE
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DZE
465,788in 2025
MAUDE reports naming product code DZE, 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 | 43 | 107 | 11 | 225 |
| 2008 | 61 | 118 | 4 | 393 |
| 2009 | 41 | 110 | 3 | 164 |
| 2010 | 34 | 162 | 3 | 360 |
| 2011 | 26 | 194 | 0 | 362 |
| 2012 | 39 | 174 | 11 | 358 |
| 2013 | 42 | 195 | 1 | 391 |
| 2014 | 36 | 265 | 7 | 1,124 |
| 2015 | 36 | 215 | 3 | 2,894 |
| 2016 | 40 | 219 | 15 | 1,116 |
| 2017 | 48 | 223 | 4 | 9,719 |
| 2018 | 41 | 200 | 4 | 12,892 |
| 2019 | 31 | 231 | 8 | 167,016 |
| 2020 | 41 | 230 | 0 | 255,524 |
| 2021 | 34 | 182 | 6 | 479,618 |
| 2022 | 34 | 243 | 0 | 483,224 |
| 2023 | 35 | 248 | 0 | 537,585 |
| 2024 | 40 | 222 | 1 | 473,629 |
| 2025 | 31 | 184 | 1 | 465,788 |
| 2026 | 15 | 194 | 2 | — |
What is it indicated for?
The Magicore System is intended to replace missing teeth to restore chewing function. The Magicore System can be placed in support of single or multiple-unit restorations including; cement retained, screw retained, or overdenture restorations, and terminal or immediate abutment support for fixed bridgework. This system is for one or two stage surgical procedures. This system is intended for delayed loading.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K212517 · printed Nov 6, 2026
Cite this page
510(k) Report. “K212517: Magicore System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K212517
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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