510(k) · Cleared
ClearedNeodent Implant for Orthodontic Anchorage
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Jjgc Industria E Comercio DE Materiais Dentarios S · OAT Implant, Endosseous, Orthodontic
Cleared on Feb 23, 2011 as substantially equivalent to K082838 (Ortholution Co., Ltd., 2008) and 2 other predicates after a 152-day review. Its family tree reaches back 9 generations to 1990.
- Decided
- Feb 23, 2011
- Review
- 152 days
- Class
- Class II
- Product code
- OAT
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 9 generations to K894844 (1990). 25 ancestors in all. No later device cites it as a predicate yet.
- Root · 9 generations backK894844 Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd. · 1990
- 5 generations between
- 3 generations backK060126 Absoanchor MicroimplantDentos, Inc. · 2006
- 2 generations backK071490 Leone Orthodontic Mini ImplantLeone S.P.A. · 2008
- 1 generation backK090476 Syntec Orthodontic Mini ScrewSyntec Scientific Corp. · 2009
- This deviceK102769 Neodent Implant for Orthodontic AnchorageJjgc Industria E Comercio DE Materiais Dentarios S · 2011
Show all 9 generations
- Root · 9 generations backK894844 Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd. · 1990
- 8 generations backK973353 Bonding BaseStraumann USA · 1997
- 7 generations backK982509 Ortho Implant and AccessoriesStraumann USA · 1998
- 6 generations backK031936 Osteomed Orthodontic Screw SystemOsteomed LP · 2004
- 5 generations backK033767 Dual Top Anchor System ScrewsJeil Medical Corporation · 2004
- 4 generations backK042965 Tomas PinDentaurum, Inc. · 2005
- 3 generations backK060126 Absoanchor MicroimplantDentos, Inc. · 2006
- 2 generations backK071490 Leone Orthodontic Mini ImplantLeone S.P.A. · 2008
- 1 generation backK090476 Syntec Orthodontic Mini ScrewSyntec Scientific Corp. · 2009
- This deviceK102769 Neodent Implant for Orthodontic AnchorageJjgc Industria E Comercio DE Materiais Dentarios S · 2011
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K894844 | Bonefit Implant System Accessories & Instruments | Straumann Institute, Ltd. | 1990 | — |
| −8 | K973353 | Bonding Base | Straumann USA | 1997 | — |
| −7 | K982509 | Ortho Implant and Accessories | Straumann USA | 1998 | — |
| −6 | K031936 | Osteomed Orthodontic Screw System | Osteomed LP | 2004 | — |
| −5 | K033767 | Dual Top Anchor System Screws | Jeil Medical Corporation | 2004 | — |
| −4 | K042965 | Tomas Pin | Dentaurum, Inc. | 2005 | — |
| −3 | K060126 | Absoanchor Microimplant | Dentos, Inc. | 2006 | — |
| −2 | K071490 | Leone Orthodontic Mini Implant | Leone S.P.A. | 2008 | — |
| −1 | K090476 | Syntec Orthodontic Mini Screw | Syntec Scientific Corp. | 2009 | — |
| 0 (this device) | K102769 | Neodent Implant for Orthodontic Anchorage | Jjgc Industria E Comercio DE Materiais Dentarios S | 2011 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1993 | 3 | 0 |
| 1994 | 2 | 0 |
| 1995 | 2 | 0 |
| 1997 | 2 | 0 |
| 1998 | 1 | 0 |
| 2000 | 1 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2008 | 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 OAT? 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 OAT device
- #1 K260268 OrthoEasy Pal; OrthoEasy Pal Long Neckscore 13.2 · 7 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 |
|---|---|---|---|
| * | K082838 | Orlus Mini ScrewSummary page 2…which has been determined by FDA to be substantially equivalent to preamendment devices: ORLUS Mini Screw from Ortholution Company, Limited, cleared under K082838, Aarhus Anchorage System from Medicon E.G., cleared under K041527, and Syntec Orthodontic Mini Screws from Sy… | 2008 |
| * | K041527 | Aarhus Anchorage SystemSummary page 2…mendment devices: ORLUS Mini Screw from Ortholution Company, Limited, cleared under K082838, Aarhus Anchorage System from Medicon E.G., cleared under K041527, and Syntec Orthodontic Mini Screws from Syntec Scientific Corporation, cleared under K090476. The inte… | 2004 |
| * | K090476 | Syntec Orthodontic Mini ScrewSummary page 2…arhus Anchorage System from Medicon E.G., cleared under K041527, and Syntec Orthodontic Mini Screws from Syntec Scientific Corporation, cleared under K090476. The intended use, design, materials and functional characteristics of the Neodent Anchor and the predicate devices ar… | 2009 |
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 21 years and passes through 9 companies; a new generation was cleared every 1.3 years on median.
- None of the 25 ancestors has a recall.
How does its category compare?
All OAT devicesOAT Implant, Endosseous, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · OAT
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OAT
224in 2021
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OAT
2in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OAT
5in 2025
MAUDE reports naming product code OAT, 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 | 6 | 104 | 2 | 2 |
| 2008 | 3 | 94 | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 1 |
| 2011 | 5 | 152 | 0 | 0 |
| 2012 | 1 | — | 0 | 3 |
| 2013 | 2 | — | 0 | 2 |
| 2014 | 1 | — | 0 | 4 |
| 2015 | 1 | — | 0 | 28 |
| 2016 | 2 | — | 0 | 12 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 1 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 3 | 289 | 0 | 38 |
| 2021 | 4 | 224 | 0 | 68 |
| 2022 | 2 | — | 0 | 84 |
| 2023 | 1 | — | 0 | 78 |
| 2024 | 2 | — | 0 | 9 |
| 2025 | 1 | — | 0 | 5 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
This product is a surgical device in the form of a temporary screw used as an aid in orthodontic movement procedures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K102769 · printed Nov 6, 2026
Cite this page
510(k) Report. “K102769: Neodent Implant for Orthodontic Anchorage.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102769
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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