510(k) · Cleared
ClearedNB Mini Implant System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Arum Dentistry Co., Ltd. · DZE Implant, Endosseous, Root-Form
Cleared on Apr 26, 2024 as substantially equivalent to K190849 (Neobiotech Co., Ltd., 2019) and 4 other predicates after a 105-day review. Its family tree reaches back 16 generations to 1990.
- Decided
- Apr 26, 2024
- Review
- 105 days
- Class
- Class II
- Product code
- DZE
- Recalls
- None
- Predicates
- 5
Its longest line of descent runs back 16 generations to K894595 (1990). 260 ancestors in all, the oldest K781060 (1978). No later device cites it as a predicate yet.
- Root · 16 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 12 generations between
- 3 generations backK160670 ET US SS Prosthetic systemOsstem Implant Co., Ltd. · 2017
- 2 generations backK182091 Osstem Abutment SystemOsstem Implant Co., Ltd. · 2019
- 1 generation backK232560 Angled AbutmentArum Dentistry Co., Ltd. · 2023
- This deviceK240091 NB Mini Implant SystemArum Dentistry Co., Ltd. · 2024
Show all 16 generations
- Root · 16 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 15 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 14 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
- 13 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
- 12 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
- 11 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
- 10 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
- 9 generations backK073247 US/SS/GS SystemOsstem Implant Co., Ltd. · 2008
- 8 generations backK081575 HU/HS/HG Prosthetic SystemOsstem Implant Co., Ltd. · 2008
- 7 generations backK100245 HS/HG Prosthetic SystemOsstem Implant Co., Ltd. · 2010
- 6 generations backK110308 Prosthetic SystemOsstem Implant Co., Ltd. · 2011
- 5 generations backK123755 Multi Angled AbutmentOsstem Implant Co., Ltd. · 2013
- 4 generations backK132067 Multi Angled Abutment SystemHiossen, Inc. · 2013
- 3 generations backK160670 ET US SS Prosthetic systemOsstem Implant Co., Ltd. · 2017
- 2 generations backK182091 Osstem Abutment SystemOsstem Implant Co., Ltd. · 2019
- 1 generation backK232560 Angled AbutmentArum Dentistry Co., Ltd. · 2023
- This deviceK240091 NB Mini Implant SystemArum Dentistry Co., Ltd. · 2024
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −16 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −15 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −14 | K993595 | Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon… | Nobel Biocare Uas, Inc. | 2000 | — |
| −13 | K011879 | 3A Dental Implant System | Osseco Biosource, Ltd. | 2002 | — |
| −12 | K051576 | Avana Dental Implant System | Osstem Co., Ltd. | 2005 | — |
| −11 | K062051 | SS System | Osstem Implant Co., Ltd. | 2006 | — |
| −10 | K063861 | GS System | Osstem Implant Co., Ltd. | 2007 | — |
| −9 | K073247 | US/SS/GS System | Osstem Implant Co., Ltd. | 2008 | — |
| −8 | K081575 | HU/HS/HG Prosthetic System | Osstem Implant Co., Ltd. | 2008 | — |
| −7 | K100245 | HS/HG Prosthetic System | Osstem Implant Co., Ltd. | 2010 | — |
| −6 | K110308 | Prosthetic System | Osstem Implant Co., Ltd. | 2011 | — |
| −5 | K123755 | Multi Angled Abutment | Osstem Implant Co., Ltd. | 2013 | — |
| −4 | K132067 | Multi Angled Abutment System | Hiossen, Inc. | 2013 | — |
| −3 | K160670 | ET US SS Prosthetic system | Osstem Implant Co., Ltd. | 2017 | — |
| −2 | K182091 | Osstem Abutment System | Osstem Implant Co., Ltd. | 2019 | — |
| −1 | K232560 | Angled Abutment | Arum Dentistry Co., Ltd. | 2023 | — |
| 0 (this device) | K240091 | NB Mini Implant System | Arum Dentistry Co., Ltd. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1978 | 1 | 0 |
| 1982 | 1 | 0 |
| 1985 | 1 | 0 |
| 1986 | 2 | 0 |
| 1987 | 2 | 0 |
| 1988 | 1 | 0 |
| 1989 | 5 | 0 |
| 1990 | 6 | 0 |
| 1991 | 1 | 0 |
| 1992 | 3 | 0 |
| 1993 | 12 | 0 |
| 1994 | 10 | 0 |
| 1995 | 10 | 0 |
| 1996 | 14 | 0 |
| 1997 | 8 | 0 |
| 1998 | 8 | 0 |
| 1999 | 10 | 0 |
| 2000 | 5 | 0 |
| 2001 | 12 | 0 |
| 2002 | 18 | 0 |
| 2003 | 17 | 0 |
| 2004 | 13 | 0 |
| 2005 | 8 | 0 |
| 2006 | 9 | 0 |
| 2007 | 14 | 0 |
| 2008 | 14 | 0 |
| 2009 | 6 | 0 |
| 2010 | 9 | 0 |
| 2011 | 6 | 0 |
| 2012 | 7 | 0 |
| 2013 | 2 | 0 |
| 2014 | 2 | 0 |
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2022 | 2 | 0 |
| 2023 | 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? (5)
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 |
|---|---|---|---|
| * | K190849 | IS-III active System_S-narrow TypeSummary page 5…Date Prepared: 04/26/2024 Predicate Devices The subject device is substantially equivalent to the following predicate and reference devices: Primary Predicate • K190849, IS-III active System by Neobiotech Co., Ltd. Reference Device • K220079, Magicore Narrow System by InnoBioSurg Co., Ltd.… | 2019 |
| * | K222131 | NB 1 SA Implant SystemSummary page 5…aling Abutments by Biomet 3i • K213506, NB 1 SA Implant System by ARUM DENTISTRY Co., Ltd. • K182091, Osstem Abutment System by Osstem Implant Co., Ltd. • K222131, NB 1 SA Implant System by ARUM DENTISTRY Co., Ltd. • K230725, NB Implant System by ARUM DENTISTRY Co., Ltd. • K232560,… | 2022 |
| * | K230725 | NB Implant SystemSummary page 5…by ARUM DENTISTRY Co., Ltd. • K182091, Osstem Abutment System by Osstem Implant Co., Ltd. • K222131, NB 1 SA Implant System by ARUM DENTISTRY Co., Ltd. • K230725, NB Implant System by ARUM DENTISTRY Co., Ltd. • K232560, Angled Abutment by ARUM DENTISTRY Co., Ltd.… | 2023 |
| * | K213506 | NB 1 SA Implant SystemSummary page 5…m by InnoBioSurg Co., Ltd. • K161604, Osstem Implant System by Osstem Implant Co., Ltd. • K173374, TSV™ BellaTek® Encode® Healing Abutments by Biomet 3i • K213506, NB 1 SA Implant System by ARUM DENTISTRY Co., Ltd. • K182091, Osstem Abutment System by Osstem Implant Co., Ltd. • K22… | 2022 |
| * | K232560 | Angled AbutmentSummary page 5…ystem by Osstem Implant Co., Ltd. • K222131, NB 1 SA Implant System by ARUM DENTISTRY Co., Ltd. • K230725, NB Implant System by ARUM DENTISTRY Co., Ltd. • K232560, Angled Abutment by ARUM DENTISTRY Co., Ltd.… | 2023 |
| † | K220079 | Magicore Narrow System | 2022 |
| † | K161604 | OSSTEM Implant System | 2016 |
| † | K173374 | TSV BellaTek Encode Healing Abutments | 2017 |
| † | K182091 | Osstem Abutment System | 2019 |
What descends from it?
No later submission names this one as a predicate yet.
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 34 years and passes through 8 companies; a new generation was cleared every 1.6 years on median.
- 29 of the 260 ancestors have a recall of any class.
How does its category compare?
All DZE devicesDZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, 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 NB Mini Implant System is indicated for use in surgical and restorative applications for placement in the mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws where the horizontal space is limited by the adjacent teeth and roots, to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient's chewing function. The NB Mini Implant System is indicated also for immediate loading when good primary stability is achieved and with appropriate occlusal loading.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K240091 · printed Nov 6, 2026
Cite this page
510(k) Report. “K240091: NB Mini Implant System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K240091
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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