510(k) · Cleared
ClearedEtii SA Fixture System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hiossen, Inc. · DZE Implant, Endosseous, Root-Form
Cleared on Jul 5, 2013 as substantially equivalent to K101096 (Hiossen, Inc., 2010) and 2 other predicates after a 234-day review. Its family tree reaches back 11 generations to 1990. 14 later devices descend from it.
- Decided
- Jul 5, 2013
- Review
- 234 days
- Class
- Class II
- Product code
- DZE
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 11 generations to K894595 (1990). 34 ancestors in all. 14 later devices descend from it, 1 citing it directly.
- Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 7 generations between
- 3 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
- 2 generations backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
- 1 generation backK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
- This deviceK123471 Etii SA Fixture SystemHiossen, Inc. · 2013
- Descendant · cites it directly · 13 of its ownK140934 Hiossen Implant SystemHiossen, Inc. · 2014
- Descendant · 2 generations on · 9 of its ownK151626 ET III Bio-SA Fixture SystemHiossen, Inc. · 2016 · Recalled
- Descendant · 2 generations on · 7 of its ownK203360 EK Implants and Abutments SystemHiossen, Inc. · 2022
- Descendant · 3 generations on · 2 of its ownK221866 S-Plant Dental Implant SystemNewton Implant Systems, Inc. · 2024
- Descendant · 2 generations on · 0 of its ownK253372 ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing…Hiossen, Inc. · 2026
Show all 11 generations
- Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 10 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 9 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
- 8 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
- 7 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
- 6 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
- 5 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
- 4 generations backK080744 HG II Fixture SystemOsstem Implant Co., Ltd. · 2008
- 3 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
- 2 generations backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
- 1 generation backK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
- This deviceK123471 Etii SA Fixture SystemHiossen, Inc. · 2013
Showing 5 of 14 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 14 · See all- K140934Hiossen Implant SystemHiossen, Inc. · 2014 · cites it directly13descendants
- K151626ET III Bio-SA Fixture SystemHiossen, Inc. · 2016 · 2 generations on9descendants
- K203360EK Implants and Abutments SystemHiossen, Inc. · 2022 · 2 generations on7descendants
- K221866S-Plant Dental Implant SystemNewton Implant Systems, Inc. · 2024 · 3 generations on2descendants
- K253372ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing AbutmentsHiossen, Inc. · 2026 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −11 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −10 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −9 | K993595 | Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon… | Nobel Biocare Uas, Inc. | 2000 | — |
| −8 | K011879 | 3A Dental Implant System | Osseco Biosource, Ltd. | 2002 | — |
| −7 | K051576 | Avana Dental Implant System | Osstem Co., Ltd. | 2005 | — |
| −6 | K062051 | SS System | Osstem Implant Co., Ltd. | 2006 | — |
| −5 | K063861 | GS System | Osstem Implant Co., Ltd. | 2007 | — |
| −4 | K080744 | HG II Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −3 | K082213 | GS Iii Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −2 | K093352 | HG Iii Fixture System | Hiossen, Inc. | 2009 | — |
| −1 | K101096 | HT Iii SA Fixture System | Hiossen, Inc. | 2010 | — |
| 0 (this device) | K123471 | Etii SA Fixture System | Hiossen, Inc. | 2013 | — |
| +1 | K140934 | Hiossen Implant System | Hiossen, Inc. | 2014 | — |
| +2 | K151626 | ET III Bio-SA Fixture System | Hiossen, Inc. | 2016 | 1 |
| +2 | K203360 | EK Implants and Abutments System | Hiossen, Inc. | 2022 | — |
| +3 | K221866 | S-Plant Dental Implant System | Newton Implant Systems, Inc. | 2024 | — |
| +2 | K253372 | ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments | Hiossen, Inc. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1993 | 1 | 0 |
| 1994 | 2 | 0 |
| 1996 | 4 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 3 | 0 |
| 2002 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2006 | 2 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2019 | 1 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 3 | 0 |
| 2025 | 1 | 0 |
| 2026 | 2 | 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? (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 |
|---|---|---|---|
| * | K101096 | HT Iii SA Fixture SystemSummary page 1…Class 11 DZE 3.4Predicate Device The ET Ill SA FIXTURE SYSTEM, HIOSSEN Inc, K 10 1096 The HOII Fixture system, HIOSSEN Inc, K090237 The HG IIIShort Fixture System, OSSTEM CO., LTD, K09 1678 4. Descripti… | 2010 |
| * | K090237 | HG II Fixture SystemSummary page 1…DZE 3.4Predicate Device The ET Ill SA FIXTURE SYSTEM, HIOSSEN Inc, K 10 1096 The HOII Fixture system, HIOSSEN Inc, K090237 The HG IIIShort Fixture System, OSSTEM CO., LTD, K09 1678 4. Description 1) The ETLI SA Fixture System is dental imp… | 2009 |
| * | K091678 | HG II Short Fixture SystemSummary page 1…Device The ET Ill SA FIXTURE SYSTEM, HIOSSEN Inc, K 10 1096 The HOII Fixture system, HIOSSEN Inc, K090237 The HG IIIShort Fixture System, OSSTEM CO., LTD, K09 1678 4. Description 1) The ETLI SA Fixture System is dental implant made of titanium metal intended to be surgically p… | 2010 |
What descends from it? (14)
See all 141 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K140934 | Hiossen Implant System | 2014 | 13 |
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 23 years and passes through 7 companies; a new generation was cleared every 1.1 years on median.
- 2 of the 34 ancestors have a recall of any class.
- Of its descendants, K140934 (Hiossen, Inc., 2014) has gone furthest, with 13 descendants of its own.
- 6 other devices also cite its predicate K101096.
How does its category compare?
All DZE devicesDZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, 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?
ETII SA Fixture system is indicated for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including; cemented retained, screw retained, or overdenture restorations, and final or temporary abutment support for fixed bridgework. It is intended for delayed loading.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K123471 · printed Nov 4, 2026
Cite this page
510(k) Report. “K123471: Etii SA Fixture System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K123471
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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