510(k) · Cleared
ClearedHT Iii 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 Oct 8, 2010 as substantially equivalent to K093352 (Hiossen, Inc., 2009) and 1 other predicate after a 171-day review. Its family tree reaches back 10 generations to 1990. 104 later devices descend from it.
- Decided
- Oct 8, 2010
- Review
- 171 days
- Class
- Class II
- Product code
- DZE
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 10 generations to K894595 (1990). 31 ancestors in all. 104 later devices descend from it, 7 citing it directly.
- Root · 10 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 6 generations between
- 3 generations backK080744 HG II Fixture SystemOsstem Implant Co., Ltd. · 2008
- 2 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
- 1 generation backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
- This deviceK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
- Descendant · cites it directly · 75 of its ownK120847 ET/SS Implant SystemOsstem Implant Co., Ltd. · 2012
- Descendant · cites it directly · 64 of its ownK121585 TS Implant SystemOsstem Implant Co., Ltd. · 2013
- Descendant · 2 generations on · 44 of its ownK140507 Hiossen Prosthetic SystemOsstem Implant Co., Ltd. · 2014
- Descendant · 2 generations on · 42 of its ownK130662 ET Prosthetic SystemOsstem Implant Co., Ltd. · 2014 · Recalled
- Descendant · 2 generations on · 38 of its ownK161689 OSSTEM Implant System - AbutmentOsstem Implant Co., Ltd. · 2017 · Recalled
Show all 10 generations
- Root · 10 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 9 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 8 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
- 7 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
- 6 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
- 5 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
- 4 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
- 3 generations backK080744 HG II Fixture SystemOsstem Implant Co., Ltd. · 2008
- 2 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
- 1 generation backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
- This deviceK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
Showing 5 of 104 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 104 · See all- K120847ET/SS Implant SystemOsstem Implant Co., Ltd. · 2012 · cites it directly75descendants
- K121585TS Implant SystemOsstem Implant Co., Ltd. · 2013 · cites it directly64descendants
- K140507Hiossen Prosthetic SystemOsstem Implant Co., Ltd. · 2014 · 2 generations on44descendants
- K130662ET Prosthetic SystemOsstem Implant Co., Ltd. · 2014 · 2 generations on42descendants
- K161689OSSTEM Implant System - AbutmentOsstem Implant Co., Ltd. · 2017 · 2 generations on38descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −9 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −8 | K993595 | Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon… | Nobel Biocare Uas, Inc. | 2000 | — |
| −7 | K011879 | 3A Dental Implant System | Osseco Biosource, Ltd. | 2002 | — |
| −6 | K051576 | Avana Dental Implant System | Osstem Co., Ltd. | 2005 | — |
| −5 | K062051 | SS System | Osstem Implant Co., Ltd. | 2006 | — |
| −4 | K063861 | GS System | Osstem Implant Co., Ltd. | 2007 | — |
| −3 | K080744 | HG II Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −2 | K082213 | GS Iii Fixture System | Osstem Implant Co., Ltd. | 2008 | — |
| −1 | K093352 | HG Iii Fixture System | Hiossen, Inc. | 2009 | — |
| 0 (this device) | K101096 | HT Iii SA Fixture System | Hiossen, Inc. | 2010 | — |
| +1 | K120847 | ET/SS Implant System | Osstem Implant Co., Ltd. | 2012 | — |
| +1 | K121585 | TS Implant System | Osstem Implant Co., Ltd. | 2013 | — |
| +2 | K140507 | Hiossen Prosthetic System | Osstem Implant Co., Ltd. | 2014 | — |
| +2 | K130662 | ET Prosthetic System | Osstem Implant Co., Ltd. | 2014 | 4 |
| +2 | K161689 | OSSTEM Implant System - Abutment | Osstem Implant Co., Ltd. | 2017 | 2 |
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 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2012 | 3 | 0 |
| 2013 | 2 | 0 |
| 2014 | 3 | 0 |
| 2015 | 3 | 0 |
| 2016 | 7 | 0 |
| 2017 | 9 | 0 |
| 2018 | 3 | 0 |
| 2019 | 2 | 0 |
| 2020 | 9 | 0 |
| 2021 | 6 | 0 |
| 2022 | 7 | 0 |
| 2023 | 20 | 0 |
| 2024 | 15 | 0 |
| 2025 | 6 | 0 |
| 2026 | 8 | 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? (2)
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 |
|---|---|---|---|
| * | K093352 | HG Iii Fixture SystemSummary page 1…Class 1I DZE 3. Predicate Device The HGII Fixture System, HiOSSEN Inc, K093352 The Straumann Standard Implant, Institut Straumann Ag, K061 176 4. Description 1) The HTUI SA F… | 2009 |
| * | K061176 | Straumann Dental ImplantsSummary page 1…DZE 3. Predicate Device The HGII Fixture System, HiOSSEN Inc, K093352 The Straumann Standard Implant, Institut Straumann Ag, K061 176 4. Description 1) The HTUI SA Fixture System is dental implant made of titanium metal intended to… | 2006 |
What descends from it? (104)
See all 1047 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 20 years and passes through 7 companies; a new generation was cleared every 1.1 years on median.
- 2 of the 31 ancestors have a recall of any class.
- Of its descendants, K120847 (Osstem Implant Co., Ltd., 2012) has gone furthest, with 75 descendants of its own.
How does its category compare?
All DZE devicesDZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, 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 HT III 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 terminal or intermediate abutment support for fixed bridgework. The HT III SA Fixture System is for single and two stage surgical procedures. It is not for immediate load.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K101096 · printed Nov 4, 2026
Cite this page
510(k) Report. “K101096: HT Iii 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/K101096
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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