510(k) Report

510(k) · Cleared

Cleared

TruAbutment DS

K172304510(k) TraditionalCleared Jan 23, 2018176-day reviewClass II21 CFR 872.3630

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Truabutment, Inc. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jan 23, 2018 as substantially equivalent to K170259 (Truabutment, 2017) after a 176-day review. Its family tree reaches back 14 generations to 1990. 8 later devices descend from it.

Decided
Jan 23, 2018
Review
176 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 14 generations to K894595 (1990). 31 ancestors in all. 8 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2006: 1 other ancestor2007: 1 other ancestor2002: 1 other ancestor1999: 1 other ancestor2001: 1 other ancestor2000: 2 other ancestors1998: 2 other ancestors1994: 3 other ancestors1997: 1 other ancestor1996: 2 other ancestors1993: 1 other ancestor2020: 2 descendants cleared2023: 4 descendants cleared2025: 2 descendants clearedReference device: K121810 · Osseospeed Angled Abutment EV · Astra Tech AB · 2013Reference device: K091756 · Nobelprocera TI Abutment · Nobel Biocare AB · 2009Reference device: K052272 · Straumann Computer Aided Restoration Service · Straumann USA · 2006Reference device: K072151 · P.004 RC Cares Titanium and Ceramic Abutments · Straumann USA · 2007 · recalledReference device: K081005 · P.004 NC Cares Titanium and Ceramic Abutments · Institut Straumann AG · 2008 · recalledReference device: K082764 · Straumann WN Cares Titanium Abutment · Institut Straumann AG · 2008K894595 · Bonefit R Screw Implants · Institut Straumann AG · 1990K984104 · Iti Dental Implant System · Straumann USA · 1999 · recalledK993595 · Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon Placement) · Nobel Biocare Uas, Inc. · 2000K011879 · 3A Dental Implant System · Osseco Biosource, Ltd. · 2002K051576 · Avana Dental Implant System · Osstem Co., Ltd. · 2005K062051 · SS System · Osstem Implant Co., Ltd. · 2006K063861 · GS System · Osstem Implant Co., Ltd. · 2007K073247 · US/SS/GS System · Osstem Implant Co., Ltd. · 2008K081575 · HU/HS/HG Prosthetic System · Osstem Implant Co., Ltd. · 2008K100245 · HS/HG Prosthetic System · Osstem Implant Co., Ltd. · 2010K110308 · Prosthetic System · Osstem Implant Co., Ltd. · 2011K123627 · ET Smartfit Abutment · Hiossen, Inc. · 2013K152559 · TruAbutment DS · Truabutment · 2016K170259 · TruAbutment DS · Truabutment · 20171990200020102020
  1. Root · 14 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 10 generations between
  3. 3 generations backK123627 ET Smartfit AbutmentHiossen, Inc. · 2013
  4. 2 generations backK152559 TruAbutment DSTruabutment · 2016
  5. 1 generation backK170259 TruAbutment DSTruabutment · 2017
  6. This deviceK172304 TruAbutment DSTruabutment, Inc. · 2018
  7. Descendant · cites it directly · 7 of its ownK183106 TruAbutment DSTruabutment, Inc. · 2020
  8. Descendant · 2 generations on · 6 of its ownK200817 URIS OMNI Narrow System & ProstheticTruabutment, Inc. · 2020
  9. Descendant · 3 generations on · 1 of its ownK231411 INNO SLA Submerged Hybrid Ti-Base SystemCowellmedi Co., Ltd. · 2023
  10. Descendant · 3 generations on · 1 of its ownK231395 INNO SLA Submerged Narrow Implant SystemCowellmedi Co., Ltd. · 2023
  11. Descendant · 4 generations on · 0 of its ownK251605 DIMPLO Implant SystemDIMPLO, Ltd. · 2025
Show all 14 generations
  1. Root · 14 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 13 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 12 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 11 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
  5. 10 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
  6. 9 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
  7. 8 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
  8. 7 generations backK073247 US/SS/GS SystemOsstem Implant Co., Ltd. · 2008
  9. 6 generations backK081575 HU/HS/HG Prosthetic SystemOsstem Implant Co., Ltd. · 2008
  10. 5 generations backK100245 HS/HG Prosthetic SystemOsstem Implant Co., Ltd. · 2010
  11. 4 generations backK110308 Prosthetic SystemOsstem Implant Co., Ltd. · 2011
  12. 3 generations backK123627 ET Smartfit AbutmentHiossen, Inc. · 2013
  13. 2 generations backK152559 TruAbutment DSTruabutment · 2016
  14. 1 generation backK170259 TruAbutment DSTruabutment · 2017
  15. This deviceK172304 TruAbutment DSTruabutment, Inc. · 2018

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2020: 22023: 42025: 2
2020high 4 (2023) · low 0 (2021)2026

Most influential descendants

Showing 5 of 8 · See all
  • K183106TruAbutment DSTruabutment, Inc. · 2020 · cites it directly7descendants
  • K200817URIS OMNI Narrow System & ProstheticTruabutment, Inc. · 2020 · 2 generations on6descendants
  • K231411INNO SLA Submerged Hybrid Ti-Base SystemCowellmedi Co., Ltd. · 2023 · 3 generations on1descendant
  • K231395INNO SLA Submerged Narrow Implant SystemCowellmedi Co., Ltd. · 2023 · 3 generations on1descendant
  • K251605DIMPLO Implant SystemDIMPLO, Ltd. · 2025 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−13K984104Iti Dental Implant SystemStraumann USA19991
−12K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−11K0118793A Dental Implant SystemOsseco Biosource, Ltd.2002—
−10K051576Avana Dental Implant SystemOsstem Co., Ltd.2005—
−9K062051SS SystemOsstem Implant Co., Ltd.2006—
−8K063861GS SystemOsstem Implant Co., Ltd.2007—
−7K073247US/SS/GS SystemOsstem Implant Co., Ltd.2008—
−6K081575HU/HS/HG Prosthetic SystemOsstem Implant Co., Ltd.2008—
−5K100245HS/HG Prosthetic SystemOsstem Implant Co., Ltd.2010—
−4K110308Prosthetic SystemOsstem Implant Co., Ltd.2011—
−3K123627ET Smartfit AbutmentHiossen, Inc.2013—
−2K152559TruAbutment DSTruabutment2016—
−1K170259TruAbutment DSTruabutment2017—
0 (this device)K172304TruAbutment DSTruabutment, Inc.2018—
+1K183106TruAbutment DSTruabutment, Inc.2020—
+2K200817URIS OMNI Narrow System & ProstheticTruabutment, Inc.2020—
+3K231411INNO SLA Submerged Hybrid Ti-Base SystemCowellmedi Co., Ltd.2023—
+3K231395INNO SLA Submerged Narrow Implant SystemCowellmedi Co., Ltd.2023—
+4K251605DIMPLO Implant SystemDIMPLO, Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199430
199620
199710
199820
199910
200020
200110
200210
200610
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202020
202340
202520
FIG. 1 — Lineage of K172304, 1990–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K170259TruAbutment DS
Summary page 4
…/2018 Predicate Devices The subject device is substantially equivalent to the following predicate device: • Primary Predicate o TruAbutment DS (K170259) • Reference Predicate o Astra Tech OsseoSpeed™ EV (K121810) o NobelProcera Ti Abutment (K091756)…
Truabutment2017—
†K121810Osseospeed Angled Abutment EVAstra Tech AB2013—
†K091756Nobelprocera TI AbutmentNobel Biocare AB2009—
†K052272Straumann Computer Aided Restoration ServiceStraumann USA2006—
†K072151P.004 RC Cares Titanium and Ceramic AbutmentsStraumann USA20071
†K081005P.004 NC Cares Titanium and Ceramic AbutmentsInstitut Straumann AG20081
†K082764Straumann WN Cares Titanium AbutmentInstitut Straumann AG2008—

Also cleared against K170259: 2 other devices →

What descends from it? (8)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K183106TruAbutment DSTruabutment, Inc.20207

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 28 years and passes through 9 companies; a new generation was cleared every 1.2 years on median.
  • 1 of the 31 ancestors has a recall of any class.
  • Of its descendants, K183106 (Truabutment, Inc., 2020) has gone furthest, with 7 descendants of its own.
  • 2 other devices also cite its predicate K170259.

How does its category compare?

All NHA devices

NHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · NHA

40in 2025

2007: 382008: 312009: 302010: 192011: 312012: 252013: 222014: 272015: 292016: 382017: 312018: 312019: 282020: 382021: 292022: 332023: 512024: 432025: 402026 (partial year): 23
2007high 51 (2023) · low 19 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHA

147in 2025

2007: 91 days median2008: 90 days median2009: 95 days median2010: 162 days median2011: 130 days median2012: 171 days median2013: 184 days median2014: 160 days median2015: 151 days median2016: 202 days median2017: 188 days median2018: 200 days median2019: 160 days median2020: 153 days median2021: 211 days median2022: 142 days median2023: 147 days median2024: 158 days median2025: 147 days median2026 (partial year): 169 days median
2007high 211 (2021) · low 90 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · NHA

1in 2025

2007: 12008: 22011: 52012: 12013: 12015: 12016: 362017: 22018: 12020: 72023: 32025: 12026 (partial year): 3
2007high 36 (2016) · low 0 (2009)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · NHA

838in 2025

2007: 12008: 82009: 302010: 612011: 562012: 52013: 1432014: 1462015: 8582016: 3142017: 5772018: 5912019: 5302020: 4582021: 5462022: 4972023: 6182024: 6352025: 838
2007high 858 (2015) · low 1 (2007)2025

MAUDE reports naming product code NHA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007389111
2008319028
20093095030
201019162061
201131130556
20122517115
2013221841143
2014271600146
2015291511858
20163820236314
2017311882577
2018312001591
2019281600530
2020381537458
2021292110546
2022331420497
2023511473618
2024431580635
2025401471838
2026231693—

What is it indicated for?

The TruAbutment DS is a patient-specific CAD/CAM abutment, directly connected to endosseous dental implants and is intended for use as an aid in prosthetic rehabilitation.

It is compatible with the following systems:

« Astra Tech OsseoSpeed™ EV 3.0, 3.6, 4.2, 4.8, 5.4 mm

* Nobel Active™ Internal Connection Implant 3.5, 4.3, 5.0, 5.5 mm

» Straumann® Bone Level Implants 3.3, 4.1, 4.8 mm

All digitally designed abutments and/or coping for use with the TruAbutment DS abutments are intended to be sent to a TruAbutment-validated milling center for manufacture.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K172304: TruAbutment DS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172304

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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