510(k) · Cleared
ClearedDESS Dental Smart Solutions
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Terrats Medical SL · NHA Abutment, Implant, Dental, Endosseous
Cleared on Jun 9, 2026 as substantially equivalent to K170588 (Terrats Medical SL, 2017) and 3 other predicates after a 110-day review. Its family tree reaches back 20 generations to 1996.
- Decided
- Jun 9, 2026
- Review
- 110 days
- Class
- Class II
- Product code
- NHA
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 20 generations to K960026 (1996). 326 ancestors in all, the oldest K781060 (1978). No later device cites it as a predicate yet.
- Root · 20 generations backK960026 Biohorizons Dental Implant SystemBioHorizons Implant Systems, Inc. · 1996
- 16 generations between
- 3 generations backK191986 DESS Dental Smart SolutionsTerrats Medical SL · 2019
- 2 generations backK212577 DESS Dental Smart SolutionsTerrats Medical SL · 2021
- 1 generation backK222269 DESS Dental Smart SolutionsTerrats Medical SL · 2022
- This deviceK260564 DESS Dental Smart SolutionsTerrats Medical SL · 2026
Show all 20 generations
- Root · 20 generations backK960026 Biohorizons Dental Implant SystemBioHorizons Implant Systems, Inc. · 1996
- 19 generations backK964330 Biohorizons Dental Implant System (Name Subject to Change)BioHorizons Implant Systems, Inc. · 1997
- 18 generations backK972313 The Maestro SystemBioHorizons Implant Systems, Inc. · 1997
- 17 generations backK020133 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 16 generations backK020645 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 15 generations backK022795 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2002
- 14 generations backK030463 Modification to the Maestro SystemBioHorizons Implant Systems, Inc. · 2003 · Recalled
- 13 generations backK032351 The Maestro System 3.0MM Diameter ImplantBioHorizons Implant Systems, Inc. · 2003
- 12 generations backK041938 Maximus OS (Overdenture System)BioHorizons Implant Systems, Inc. · 2004 · Recalled
- 11 generations backK063364 Alpha Bio Dental Implant SystemAlpha-Bio Tec, Ltd. · 2007
- 10 generations backK081653 Mdi Mii One-Piece Implant, 2.9MMImtec Corp. · 2008 · Recalled
- 9 generations backK123022 Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2013
- 8 generations backK133510 Neodent Implant SystemJj Industria E Comercio DE Materiais Dentarios SA · 2014
- 7 generations backK133592 Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua…Neodent USA, Inc. · 2014
- 6 generations backK150367 Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2015
- 5 generations backK170588 DESS Dental Smart SolutionsTerrats Medical SL · 2017
- 4 generations backK173908 DESS Dental Smart SolutionsTerrats Medical SL · 2018
- 3 generations backK191986 DESS Dental Smart SolutionsTerrats Medical SL · 2019
- 2 generations backK212577 DESS Dental Smart SolutionsTerrats Medical SL · 2021
- 1 generation backK222269 DESS Dental Smart SolutionsTerrats Medical SL · 2022
- This deviceK260564 DESS Dental Smart SolutionsTerrats Medical SL · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −20 | K960026 | Biohorizons Dental Implant System | BioHorizons Implant Systems, Inc. | 1996 | — |
| −19 | K964330 | Biohorizons Dental Implant System (Name Subject to Change) | BioHorizons Implant Systems, Inc. | 1997 | — |
| −18 | K972313 | The Maestro System | BioHorizons Implant Systems, Inc. | 1997 | — |
| −17 | K020133 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −16 | K020645 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −15 | K022795 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2002 | — |
| −14 | K030463 | Modification to the Maestro System | BioHorizons Implant Systems, Inc. | 2003 | 1 |
| −13 | K032351 | The Maestro System 3.0MM Diameter Implant | BioHorizons Implant Systems, Inc. | 2003 | — |
| −12 | K041938 | Maximus OS (Overdenture System) | BioHorizons Implant Systems, Inc. | 2004 | 2 |
| −11 | K063364 | Alpha Bio Dental Implant System | Alpha-Bio Tec, Ltd. | 2007 | — |
| −10 | K081653 | Mdi Mii One-Piece Implant, 2.9MM | Imtec Corp. | 2008 | 1 |
| −9 | K123022 | Neodent Implant System | Jjgc Industria E Comercio DE Materiais Dentarios S | 2013 | — |
| −8 | K133510 | Neodent Implant System | Jj Industria E Comercio DE Materiais Dentarios SA | 2014 | — |
| −7 | K133592 | Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua, Titamax Smart… | Neodent USA, Inc. | 2014 | — |
| −6 | K150367 | Neodent Implant System | Jjgc Industria E Comercio DE Materiais Dentarios S | 2015 | — |
| −5 | K170588 | DESS Dental Smart Solutions | Terrats Medical SL | 2017 | — |
| −4 | K173908 | DESS Dental Smart Solutions | Terrats Medical SL | 2018 | — |
| −3 | K191986 | DESS Dental Smart Solutions | Terrats Medical SL | 2019 | — |
| −2 | K212577 | DESS Dental Smart Solutions | Terrats Medical SL | 2021 | — |
| −1 | K222269 | DESS Dental Smart Solutions | Terrats Medical SL | 2022 | — |
| 0 (this device) | K260564 | DESS Dental Smart Solutions | Terrats Medical SL | 2026 | — |
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 | 14 | 0 |
| 2009 | 13 | 0 |
| 2010 | 10 | 0 |
| 2011 | 10 | 0 |
| 2012 | 5 | 0 |
| 2013 | 3 | 0 |
| 2014 | 3 | 0 |
| 2015 | 2 | 0 |
| 2017 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 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 30.6 · 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? (4)
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 |
|---|---|---|---|
| * | K170588 | DESS Dental Smart SolutionsSummary page 6…Classification Panel Dental Products Panel Reviewing Division DHT1B: Division of Dental and ENT Devices PREDICATE DEVICE INFORMATION Primary Predicate Device K170588, DESS Dental Smart Solutions, Terrats Medical SL Reference Devices K222269, DESS Dental Smart Solutions, Terrats Medical SL… | 2017 |
| * | K222269 | DESS Dental Smart SolutionsSummary page 6…ivision of Dental and ENT Devices PREDICATE DEVICE INFORMATION Primary Predicate Device K170588, DESS Dental Smart Solutions, Terrats Medical SL Reference Devices K222269, DESS Dental Smart Solutions, Terrats Medical SL Page 1 of 10 Traditional 510(k) Premarket Notification… | 2022 |
| * | K240208 | DESS Dental Smart SolutionsSummary page 7…DESS Dental Smart Solutions 510(k) Summary K260564 K240208, DESS Dental Smart Solutions, Terrats Medical SL K120954, Nobel Procera PEEK Abutments, Nobel Biocare AB Reference Devices for… | 2024 |
| * | K120954 | Nobelprocera Peek AbutmentsSummary page 7…0(k) Summary K260564 K240208, DESS Dental Smart Solutions, Terrats Medical SL K120954, Nobel Procera PEEK Abutments, Nobel Biocare AB Reference Devices for OEM implant body clearances K210117, Paltop Narrow Impla… | 2013 |
| † | K210117 | Paltop Narrow Implant | 2021 |
| † | K223814 | Genesis ACTIVE Implant System | 2023 |
| † | K243983 | Paltop Dental Implant System | 2025 |
| † | K232740 | Paltop Short Implants | 2024 |
| † | K220200 | Paltop Conical Implant System | 2022 |
| † | K240966 | Prima Plus Conical Implant System | 2024 |
| † | K142260 | NobelActive | 2015 |
| † | K102436 | Nobel Active 3.0 | 2010 |
| † | K173418 | NobelParallel Conical Connection | 2019 |
| † | K050705 | Tiunite Implants | 2005 |
| † | K050406 | Nobelspeedy Implants | 2005 |
| † | K022562 | Various Branemark System Implants-Immediate Function Indication | 2002 |
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 30 years and passes through 7 companies; a new generation was cleared every 11 months on median.
- 44 of the 326 ancestors have a recall of any class.
- 15 other devices also cite its predicate K170588.
How does its category compare?
All NHA devicesNHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, 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?
DESS Dental Smart Solutions abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for prosthetic restorations. All digitally designed custom abutments for use with DESS Bases or Blanks are to be sent to a Terrats Medical validated milling center for manufacture. The PEEK Abutments are premanufactured prosthetic component directly connected to the endosseous dental implants…
Read the full statement (201 words)
DESS Dental Smart Solutions abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for prosthetic restorations.
All digitally designed custom abutments for use with DESS Bases or Blanks are to be sent to a Terrats Medical validated milling center for manufacture.
The PEEK Abutments are premanufactured prosthetic component directly connected to the endosseous dental implants and are intended for provisional use up to 180 days as an aid in prosthetic rehabilitation.
Compatible Implant Systems
Implant Compatibility (Connection) Implant Body Diameter, mm Implant Platform, mm
NobelActive® NobelReplace/NobelParallel Conical 3.0 3.0
3.5 NP (3.5)
4.3, 5.0 RP (3.9)
5.5 WP (5.1)
NobelReplace® Trilobe 3.5 NP (3.5)
4.3 RP (4.3)
5.0 WP
Nobel Brånemark System® 3.3 NP
3.75, 4.0 RP
5.0 WP
Keystone Paltop Dynamic (Internal Hex) 3.0, 3.25 NP (3.25)
PALTOP ADVANCED CLASSIC (Internal Hex) 3.25 NP (3.25)
PALTOP ADVANCED PLUS (Internal Hex) 3.0, 3.25 NP (3.25)
Keystone Paltop Dynamic Conical (Internal conical) 3.25, 3.75, 4.2, 5.0 CC (3.25/3.75/4.2/5.0)
Genesis Active (Internal conical) 3.5, 3.8, 4.5, 5.5 CC (3.5/3.8/4.5/5.5)
PALTOP Implants (Internal conical) 3.25 NP (3.25)
Keystone Prima Plus Conical (Internal conical) 3.5, 4.1, 5.0, 6.0 CC (3.5, 4.1, 5.0, 6.0)
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K260564 · printed Nov 6, 2026
Cite this page
510(k) Report. “K260564: DESS Dental Smart Solutions.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K260564
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded Oct 30, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026