510(k) · Cleared
ClearedSQ IS System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Neobiotech Co., Ltd. · DZE Implant, Endosseous, Root-Form
Cleared on Jul 16, 2009 as substantially equivalent to K063861 (Osstem Implant Co., Ltd., 2007) and 2 other predicates after a 112-day review. Its family tree reaches back 8 generations to 1990. 55 later devices descend from it.
- Decided
- Jul 16, 2009
- Review
- 112 days
- Class
- Class II
- Product code
- DZE
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 8 generations to K894595 (1990). 24 ancestors in all. 55 later devices descend from it, 5 citing it directly.
- Root · 8 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 7 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 6 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
- 5 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
- 4 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
- 3 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
- 2 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
- 1 generation backK073465 US/GS Ultra Wide SystemOsstem Implant Co., Ltd. · 2008
- This deviceK090825 SQ IS SystemNeobiotech Co., Ltd. · 2009
- Descendant · cites it directly · 34 of its ownK113554 Cmi Implant IS SystemNeobiotech Co., Ltd. · 2012
- Descendant · 2 generations on · 23 of its ownK181138 IS-III active SystemNeobiotech Co., Ltd. · 2018
- Descendant · cites it directly · 14 of its ownK120951 Smartbuilder SystemOsstem Implant Co., Ltd. · 2012
- Descendant · 2 generations on · 9 of its ownK120503 Cmi Implant IS II ActiveNeobiotech Co., Ltd. · 2012
- Descendant · 3 generations on · 8 of its ownK211090 ZENEX Implant SystemIzenimplant Co., Ltd. · 2022
Showing 5 of 55 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 55 · See all- K113554Cmi Implant IS SystemNeobiotech Co., Ltd. · 2012 · cites it directly34descendants
- K181138IS-III active SystemNeobiotech Co., Ltd. · 2018 · 2 generations on23descendants
- K120951Smartbuilder SystemOsstem Implant Co., Ltd. · 2012 · cites it directly14descendants
- K120503Cmi Implant IS II ActiveNeobiotech Co., Ltd. · 2012 · 2 generations on9descendants
- K211090ZENEX Implant SystemIzenimplant Co., Ltd. · 2022 · 3 generations on8descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −7 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −6 | K993595 | Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon… | Nobel Biocare Uas, Inc. | 2000 | — |
| −5 | K011879 | 3A Dental Implant System | Osseco Biosource, Ltd. | 2002 | — |
| −4 | K051576 | Avana Dental Implant System | Osstem Co., Ltd. | 2005 | — |
| −3 | K062051 | SS System | Osstem Implant Co., Ltd. | 2006 | — |
| −2 | K063861 | GS System | Osstem Implant Co., Ltd. | 2007 | — |
| −1 | K073465 | US/GS Ultra Wide System | Osstem Implant Co., Ltd. | 2008 | — |
| 0 (this device) | K090825 | SQ IS System | Neobiotech Co., Ltd. | 2009 | — |
| +1 | K113554 | Cmi Implant IS System | Neobiotech Co., Ltd. | 2012 | — |
| +2 | K181138 | IS-III active System | Neobiotech Co., Ltd. | 2018 | — |
| +1 | K120951 | Smartbuilder System | Osstem Implant Co., Ltd. | 2012 | — |
| +2 | K120503 | Cmi Implant IS II Active | Neobiotech Co., Ltd. | 2012 | — |
| +3 | K211090 | ZENEX Implant System | Izenimplant Co., Ltd. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1993 | 1 | 0 |
| 1994 | 2 | 0 |
| 1996 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 2000 | 2 | 0 |
| 2001 | 1 | 0 |
| 2002 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 2 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 2 | 0 |
| 2011 | 1 | 0 |
| 2012 | 3 | 0 |
| 2013 | 2 | 0 |
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 6 | 0 |
| 2019 | 2 | 0 |
| 2020 | 8 | 0 |
| 2021 | 2 | 0 |
| 2022 | 6 | 0 |
| 2023 | 8 | 0 |
| 2024 | 5 | 0 |
| 2025 | 5 | 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 |
|---|---|---|---|
| * | K063861 | GS SystemSummary page 2…g ASTM and ISO standards. Predicate Devices The subject device is substantially equivalent to the following predicate devices: · GS System (Osstem Co., Ltd.; K063861) * GS Ultra Wide System (Osstem Co., Ltd.; K073465) * Rescue Internal Implant System (Megagen Co., Ltd.; K073058)… | 2007 |
| * | K073465 | US/GS Ultra Wide SystemSummary page 2…ct device is substantially equivalent to the following predicate devices: · GS System (Osstem Co., Ltd.; K063861) * GS Ultra Wide System (Osstem Co., Ltd.; K073465) * Rescue Internal Implant System (Megagen Co., Ltd.; K073058) Comparison to Predicate Devices Testing and other comp… | 2008 |
| * | K073058 | Rescue Internal Implant SystemSummary page 2…ces: · GS System (Osstem Co., Ltd.; K063861) * GS Ultra Wide System (Osstem Co., Ltd.; K073465) * Rescue Internal Implant System (Megagen Co., Ltd.; K073058) Comparison to Predicate Devices Testing and other comparisons have established that the subject of SQ IS System is substant… | 2008 |
What descends from it? (55)
See all 555 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 19 years and passes through 7 companies; a new generation was cleared every 1.3 years on median.
- 1 of the 24 ancestors has a recall of any class.
- Of its descendants, K113554 (Neobiotech Co., Ltd., 2012) has gone furthest, with 34 descendants of its own.
- 9 other devices also cite its predicate K063861.
How does its category compare?
All DZE devicesDZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, 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 SQ IS 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. IS System is dedicated for two stage surgical procedures and for immediate loading when there is good primary stability and an appropriate occlusal load. Also, implants with diameters larger than 5mm are indicated for molar regions.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K090825 · printed Nov 4, 2026
Cite this page
510(k) Report. “K090825: SQ IS System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K090825
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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