510(k) · Cleared
ClearedAdin Customized Abutments
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Adin Dental Implant Systems, Ltd. · NHA Abutment, Implant, Dental, Endosseous
Cleared on Oct 17, 2025 as substantially equivalent to K221301 (Terrats Medical SL, 2023) and 6 other predicates after a 268-day review. Its family tree reaches back 21 generations to 1996.
- Decided
- Oct 17, 2025
- Review
- 268 days
- Class
- Class II
- Product code
- NHA
- Recalls
- None
- Predicates
- 7
Its longest line of descent runs back 21 generations to K960026 (1996). 337 ancestors in all, the oldest K781060 (1978). No later device cites it as a predicate yet.
- Root · 21 generations backK960026 Biohorizons Dental Implant SystemBioHorizons Implant Systems, Inc. · 1996
- 17 generations between
- 3 generations backK203464 DESS Dental Smart SolutionsTerrats Medical SL · 2021
- 2 generations backK222288 DESS Dental Smart SolutionsTerrats Medical SL · 2022
- 1 generation backK221301 DESS Dental Smart SolutionsTerrats Medical SL · 2023
- This deviceK250178 Adin Customized AbutmentsAdin Dental Implant Systems, Ltd. · 2025
Show all 21 generations
- Root · 21 generations backK960026 Biohorizons Dental Implant SystemBioHorizons Implant Systems, Inc. · 1996
- 20 generations backK964330 Biohorizons Dental Implant System (Name Subject to Change)BioHorizons Implant Systems, Inc. · 1997
- 19 generations backK972313 The Maestro SystemBioHorizons Implant Systems, Inc. · 1997
- 18 generations backK020133 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 17 generations backK020645 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 16 generations backK022795 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 15 generations backK030463 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2003 · Recalled
- 14 generations backK032351 The Maestro System 3.0MM Diameter ImplantBioHorizons Implant Systems, Inc. · 2003
- 13 generations backK041938 Maximus OS (Overdenture System)BioHorizons Implant Systems, Inc. · 2004 · Recalled
- 12 generations backK063364 Alpha Bio Dental Implant SystemAlpha-Bio Tec, Ltd. · 2007
- 11 generations backK081653 Mdi Mii One-Piece Implant, 2.9MMImtec Corp. · 2008 · Recalled
- 10 generations backK123022 Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2013
- 9 generations backK133510 Neodent Implant SystemJj Industria E Comercio DE Materiais Dentarios SA · 2014
- 8 generations backK133592 Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua…Neodent USA, Inc. · 2014
- 7 generations backK150367 Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2015
- 6 generations backK170588 DESS Dental Smart SolutionsTerrats Medical SL · 2017
- 5 generations backK173908 DESS Dental Smart SolutionsTerrats Medical SL · 2018
- 4 generations backK191986 DESS Dental Smart SolutionsTerrats Medical SL · 2019
- 3 generations backK203464 DESS Dental Smart SolutionsTerrats Medical SL · 2021
- 2 generations backK222288 DESS Dental Smart SolutionsTerrats Medical SL · 2022
- 1 generation backK221301 DESS Dental Smart SolutionsTerrats Medical SL · 2023
- This deviceK250178 Adin Customized AbutmentsAdin Dental Implant Systems, Ltd. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −21 | K960026 | Biohorizons Dental Implant System | BioHorizons Implant Systems, Inc. | 1996 | — |
| −20 | K964330 | Biohorizons Dental Implant System (Name Subject to Change) | BioHorizons Implant Systems, Inc. | 1997 | — |
| −19 | K972313 | The Maestro System | BioHorizons Implant Systems, Inc. | 1997 | — |
| −18 | K020133 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −17 | K020645 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −16 | K022795 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −15 | K030463 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2003 | 1 |
| −14 | K032351 | The Maestro System 3.0MM Diameter Implant | BioHorizons Implant Systems, Inc. | 2003 | — |
| −13 | K041938 | Maximus OS (Overdenture System) | BioHorizons Implant Systems, Inc. | 2004 | 2 |
| −12 | K063364 | Alpha Bio Dental Implant System | Alpha-Bio Tec, Ltd. | 2007 | — |
| −11 | K081653 | Mdi Mii One-Piece Implant, 2.9MM | Imtec Corp. | 2008 | 1 |
| −10 | K123022 | Neodent Implant System | Jjgc Industria E Comercio DE Materiais Dentarios S | 2013 | — |
| −9 | K133510 | Neodent Implant System | Jj Industria E Comercio DE Materiais Dentarios SA | 2014 | — |
| −8 | K133592 | Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua, Titamax Smart… | Neodent USA, Inc. | 2014 | — |
| −7 | K150367 | Neodent Implant System | Jjgc Industria E Comercio DE Materiais Dentarios S | 2015 | — |
| −6 | K170588 | DESS Dental Smart Solutions | Terrats Medical SL | 2017 | — |
| −5 | K173908 | DESS Dental Smart Solutions | Terrats Medical SL | 2018 | — |
| −4 | K191986 | DESS Dental Smart Solutions | Terrats Medical SL | 2019 | — |
| −3 | K203464 | DESS Dental Smart Solutions | Terrats Medical SL | 2021 | — |
| −2 | K222288 | DESS Dental Smart Solutions | Terrats Medical SL | 2022 | — |
| −1 | K221301 | DESS Dental Smart Solutions | Terrats Medical SL | 2023 | — |
| 0 (this device) | K250178 | Adin Customized Abutments | Adin Dental Implant Systems, Ltd. | 2025 | — |
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 | 7 | 0 |
| 1991 | 1 | 0 |
| 1992 | 4 | 0 |
| 1993 | 12 | 0 |
| 1994 | 12 | 0 |
| 1995 | 15 | 0 |
| 1996 | 16 | 0 |
| 1997 | 7 | 0 |
| 1998 | 8 | 0 |
| 1999 | 11 | 0 |
| 2000 | 11 | 0 |
| 2001 | 18 | 0 |
| 2002 | 19 | 0 |
| 2003 | 17 | 0 |
| 2004 | 16 | 0 |
| 2005 | 14 | 0 |
| 2006 | 17 | 0 |
| 2007 | 24 | 0 |
| 2008 | 15 | 0 |
| 2009 | 13 | 0 |
| 2010 | 10 | 0 |
| 2011 | 10 | 0 |
| 2012 | 6 | 0 |
| 2013 | 3 | 0 |
| 2014 | 4 | 0 |
| 2015 | 2 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2022 | 2 | 0 |
| 2023 | 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 NHA? 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 NHA device
- #1 K222288 DESS Dental Smart Solutionsscore 30.7 · 19 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (7)
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 |
|---|---|---|---|
| * | K221301 | DESS Dental Smart SolutionsSummary page 5…iratory, ENT and Dental Devices) Reviewing Division Division of Health Technology 1 B, Dental and ENT Devices PREDICATE DEVICE INFORMATION Primary Predicate Device K221301, DESS Dental Smart Solutions, Terrats Medical SL. Reference Devices K223714, UniFit Dental Implant System, Adin Dental Implant S… | 2023 |
| * | K223714 | UniFit Dental Implant SystemSummary page 5…chnology 1 B, Dental and ENT Devices PREDICATE DEVICE INFORMATION Primary Predicate Device K221301, DESS Dental Smart Solutions, Terrats Medical SL. Reference Devices K223714, UniFit Dental Implant System, Adin Dental Implant Systems Ltd. K112585, Touareg CloseFit Dental Implant System, Adin Dental Impl… | 2023 |
| * | K112585 | Touareg Closefit Dental Impant SystemSummary page 5…ary Predicate Device K221301, DESS Dental Smart Solutions, Terrats Medical SL. Reference Devices K223714, UniFit Dental Implant System, Adin Dental Implant Systems Ltd. K112585, Touareg CloseFit Dental Implant System, Adin Dental Implant Systems Ltd. K081751, Adin Dental Implants System, Adin Dental Impla… | 2012 |
| * | K081751 | Adin Dental Implants SystemSummary page 5…ference Devices K223714, UniFit Dental Implant System, Adin Dental Implant Systems Ltd. K112585, Touareg CloseFit Dental Implant System, Adin Dental Implant Systems Ltd. K081751, Adin Dental Implants System, Adin Dental Implant Systems Ltd. 510(k) Summary… | 2008 |
| * | K223677 | Titanium Abutment Blank Nobel Biocare N1 TCCSummary page 6…Adin Customized Abutments Page 2 of 11 K250178 K223677, Titanium Abutment Blank Nobel Biocare N1™ TCC, Nobel Biocare AB K153111, Touareg CloseFit UNP 2.75mmD, Adin Dental Implant Syste… | 2023 |
| * | K153111 | TOUAREG CloseFit™ UNP 2.75mmDSummary page 6…K250178 K223677, Titanium Abutment Blank Nobel Biocare N1™ TCC, Nobel Biocare AB K153111, Touareg CloseFit UNP 2.75mmD, Adin Dental Implant Systems Ltd. K140293, Touareg NP CloseFit Dental Implants System, Adin Dental… | 2016 |
| * | K140293 | Touareg NP Closefit Dental Implants SystemSummary page 6…K250178 K223677, Titanium Abutment Blank Nobel Biocare N1™ TCC, Nobel Biocare AB K153111, Touareg CloseFit UNP 2.75mmD, Adin Dental Implant Systems Ltd. K140293, Touareg NP CloseFit Dental Implants System, Adin Dental Implant Systems Ltd. INDICATIONS FOR USE STATEMENT Adin Customized Abut… | 2014 |
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 29 years and passes through 8 companies; a new generation was cleared every 10 months on median.
- 44 of the 337 ancestors have a recall of any class.
- 2 other devices also cite its predicate K221301.
How does its category compare?
All NHA devicesNHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · NHA
40in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NHA
147in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NHA
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NHA
838in 2025
MAUDE reports naming product code NHA, 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 | 38 | 91 | 1 | 1 |
| 2008 | 31 | 90 | 2 | 8 |
| 2009 | 30 | 95 | 0 | 30 |
| 2010 | 19 | 162 | 0 | 61 |
| 2011 | 31 | 130 | 5 | 56 |
| 2012 | 25 | 171 | 1 | 5 |
| 2013 | 22 | 184 | 1 | 143 |
| 2014 | 27 | 160 | 0 | 146 |
| 2015 | 29 | 151 | 1 | 858 |
| 2016 | 38 | 202 | 36 | 314 |
| 2017 | 31 | 188 | 2 | 577 |
| 2018 | 31 | 200 | 1 | 591 |
| 2019 | 28 | 160 | 0 | 530 |
| 2020 | 38 | 153 | 7 | 458 |
| 2021 | 29 | 211 | 0 | 546 |
| 2022 | 33 | 142 | 0 | 497 |
| 2023 | 51 | 147 | 3 | 618 |
| 2024 | 43 | 158 | 0 | 635 |
| 2025 | 40 | 147 | 1 | 838 |
| 2026 | 23 | 169 | 3 | — |
What is it indicated for?
Adin Customized Abutments are intended for use with Adin dental implants in partially or fully edentulous mandibles and maxillae, as a support for single-unit or multiple-unit screw-retained or cement-retained restorations.
All digitally designed abutments for use with Adin Ti-base and Adin Ti-blanks are intended to be sent to an FDA-registered Adin Dental Implants validated milling center for manufacture or to be manufactured according to the digital dentistry workflow, which integrates multiple components: scans from desktop and intraoral scanners, CAD and CAM software and a milling machine with associated accessories.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K250178 · printed Nov 4, 2026
Cite this page
510(k) Report. “K250178: Adin Customized Abutments.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K250178
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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