510(k) · Cleared
ClearedAnkylos Syncone Abutment 5(Degree)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dentsply International, Inc. · NHA Abutment, Implant, Dental, Endosseous
Cleared on Jan 22, 2014 as substantially equivalent to K041509 (Friadent GmbH, 2004) and 1 other predicate after a 231-day review. Its family tree reaches back 7 generations to 1990. 1 later device descends from it.
- Decided
- Jan 22, 2014
- Review
- 231 days
- Class
- Class II
- Product code
- NHA
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 7 generations to K894595 (1990). 34 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 7 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
- 6 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
- 5 generations backK992937 Dental ImplantNobel Biocare Uas, Inc. · 2000 · Recalled
- 4 generations backK013067 Frialoc Dental Implant SystemFriadent GmbH · 2002
- 3 generations backK021318 Xive Dental Implant SystemFriadent GmbH · 2002
- 2 generations backK032158 Xive Dental Implant System MultipleFriadent GmbH · 2003
- 1 generation backK041509 Ankylos Dental Implant SystemFriadent GmbH · 2004
- This deviceK131644 Ankylos Syncone Abutment 5(Degree)Dentsply International, Inc. · 2014
- Descendant · cites it directly · 0 of its ownK151439 Atlantis IsusDentsply International, Inc. · 2016
Most influential descendants
Showing 1 of 1 · See all- K151439Atlantis IsusDentsply International, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K894595 | Bonefit R Screw Implants | Institut Straumann AG | 1990 | — |
| −6 | K984104 | Iti Dental Implant System | Straumann USA | 1999 | 1 |
| −5 | K992937 | Dental Implant | Nobel Biocare Uas, Inc. | 2000 | 1 |
| −4 | K013067 | Frialoc Dental Implant System | Friadent GmbH | 2002 | — |
| −3 | K021318 | Xive Dental Implant System | Friadent GmbH | 2002 | — |
| −2 | K032158 | Xive Dental Implant System Multiple | Friadent GmbH | 2003 | — |
| −1 | K041509 | Ankylos Dental Implant System | Friadent GmbH | 2004 | — |
| 0 (this device) | K131644 | Ankylos Syncone Abutment 5(Degree) | Dentsply International, Inc. | 2014 | — |
| +1 | K151439 | Atlantis Isus | Dentsply International, Inc. | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1993 | 3 | 0 |
| 1994 | 2 | 0 |
| 1995 | 1 | 0 |
| 1996 | 6 | 0 |
| 1997 | 2 | 0 |
| 1998 | 1 | 0 |
| 2000 | 2 | 0 |
| 2002 | 5 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2008 | 1 | 0 |
| 2012 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 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 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? (2)
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 |
|---|---|---|---|
| * | K041509 | Ankylos Dental Implant SystemSummary page 1…butmcm . QTR Numbet: 872 3630 « Product:Code:. NHA Predicate-Dévice: . ANKYLOS" SynCone Abulmenls 4° and 6°,.cleared as' part. of the ANKYLOS ‘Dental ]mplant System- (K041 509) ‘ . An«vled ANKYL@S Baiance Base Abutments (K 122268) bescr;gnon of Device: The ANKYLOS% Q)nCone Abutinent 59 i$-an: endosseous… | 2004 |
| * | K122268 | Angled Xive MP Abutment, Angled AnkylosSummary page 1…redicate-Dévice: . ANKYLOS" SynCone Abulmenls 4° and 6°,.cleared as' part. of the ANKYLOS ‘Dental ]mplant System- (K041 509) ‘ . An«vled ANKYL@S Baiance Base Abutments (K 122268) bescr;gnon of Device: The ANKYLOS% Q)nCone Abutinent 59 i$-an: endosseous dental implant abutment wlnch prowdes a platforim- f… | 2012 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K151439 | Atlantis Isus | 2016 | 0 |
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 24 years and passes through 5 companies; a new generation was cleared every 1.1 years on median.
- 3 of the 34 ancestors have a recall of any class.
- Of its descendants, K151439 (Dentsply International, Inc., 2016) has gone furthest, with 0 descendants of its own.
- 9 other devices also cite its predicate K041509.
How does its category compare?
All NHA devicesNHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, 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?
SynCone® Abutments on osseointegrated Implants
Anchorage of dentures retained by taper friction and supported by ANKYLOS® implants
SynCone™ Abutments for immediate loading
Immediate loading of an implant supported prosthesis in an edentulous mandible supported by 4 ANXYLOS® implants off at least 11 mm in length and placed interfaraminally.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K131644 · printed Nov 5, 2026
Cite this page
510(k) Report. “K131644: Ankylos Syncone Abutment 5(Degree).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131644
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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