510(k) Report

510(k) · Cleared

Cleared

Inclusive Titanium Abutments Compatible with Straumann Tissue Level Implants

K141211510(k) TraditionalCleared Oct 22, 2014166-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

Prismatik Dentalcraft, Inc. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Oct 22, 2014 as substantially equivalent to K033243 (Straumann USA, 2003) and 1 other predicate after a 166-day review. Its family tree reaches back 9 generations to 1990. 1 later device descends from it.

Decided
Oct 22, 2014
Review
166 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K894595 (1990). 70 ancestors in all, the oldest K871863 (1987). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 2 other ancestors2006: 1 other ancestor2004: 2 other ancestors2002: 4 other ancestors2001: 4 other ancestors1999: 3 other ancestors1998: 3 other ancestors1996: 8 other ancestors1994: 9 other ancestors2005: 1 other ancestor1997: 4 other ancestors1995: 6 other ancestors1990: 1 other ancestor1989: 1 other ancestor1987: 1 other ancestor1993: 10 other ancestors1991: 1 other ancestor2015: 1 descendant clearedK894595 · 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. · 2000K023113 · Replace Tiunite Endosseous Implant · Nobel Biocare Uas, Inc. · 2002 · recalledK041661 · Nobel Biocare Endosseous Implants · Nobel Biocare Uas, Inc. · 2004K050258 · Groovy Implants · Nobel Biocare AB · 2005 · recalledK061003 · SFB & CFB Implants · Nobel Biocare AB · 2006K071370 · Nobelactive Internal Connection Implant · Nobel Biocare AB · 2007 · recalledK083192 · Inclusive Titanium Abutment Blanks · Inclusive Dental Solutions · 20091990200020102020
  1. Root · 9 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 5 generations between
  3. 3 generations backK061003 SFB & CFB ImplantsNobel Biocare AB · 2006
  4. 2 generations backK071370 Nobelactive Internal Connection ImplantNobel Biocare AB · 2007 · Recalled
  5. 1 generation backK083192 Inclusive Titanium Abutment BlanksInclusive Dental Solutions · 2009
  6. This deviceK141211 Inclusive Titanium Abutments Compatible with Straumann Tissue Level…Prismatik Dentalcraft, Inc. · 2014
  7. Descendant · cites it directly · 0 of its ownK151798 Inclusive Titanium Abutments compatible with: Straumann synOcta…Prismatik Dentalcraft, Inc. · 2015
Show all 9 generations
  1. Root · 9 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 8 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 7 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 6 generations backK023113 Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc. · 2002 · Recalled
  5. 5 generations backK041661 Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc. · 2004
  6. 4 generations backK050258 Groovy ImplantsNobel Biocare AB · 2005 · Recalled
  7. 3 generations backK061003 SFB & CFB ImplantsNobel Biocare AB · 2006
  8. 2 generations backK071370 Nobelactive Internal Connection ImplantNobel Biocare AB · 2007 · Recalled
  9. 1 generation backK083192 Inclusive Titanium Abutment BlanksInclusive Dental Solutions · 2009
  10. This deviceK141211 Inclusive Titanium Abutments Compatible with Straumann Tissue Level…Prismatik Dentalcraft, Inc. · 2014

Most influential descendants

Showing 1 of 1 · See all
  • K151798Inclusive Titanium Abutments compatible with: Straumann synOcta Implant SystemPrismatik Dentalcraft, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−8K984104Iti Dental Implant SystemStraumann USA19991
−7K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−6K023113Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc.200227
−5K041661Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc.2004—
−4K050258Groovy ImplantsNobel Biocare AB200528
−3K061003SFB & CFB ImplantsNobel Biocare AB2006—
−2K071370Nobelactive Internal Connection ImplantNobel Biocare AB20074
−1K083192Inclusive Titanium Abutment BlanksInclusive Dental Solutions2009—
0 (this device)K141211Inclusive Titanium Abutments Compatible with Straumann Tissue Level ImplantsPrismatik Dentalcraft, Inc.2014—
+1K151798Inclusive Titanium Abutments compatible with: Straumann synOcta Implant SystemPrismatik Dentalcraft, Inc.2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198910
199010
199110
1993100
199490
199560
199680
199740
199830
199930
200140
200240
200320
200420
200510
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of K141211, 1990–2015Source: 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K033243Iti Synocta Meso Abutments
Summary page 5
…Review Panel: Dental C. IDENTIFICATION OF PREDICATE DEVICE Trade/Proprietary Name: ITI synOcta Meso Abutments (K033243) Inclusive Titanium Abutment Blanks (K083192) D. DEVICE DESCRIPTION Inclusive Titaniu…
Straumann USA2003—
*K083192Inclusive Titanium Abutment Blanks
Summary page 5
…ATION OF PREDICATE DEVICE Trade/Proprietary Name: ITI synOcta Meso Abutments (K033243) Inclusive Titanium Abutment Blanks (K083192) D. DEVICE DESCRIPTION Inclusive Titanium Abutments are endosseous implant abutments which are placed into the dent…
Inclusive Dental Solutions2009—

Also cleared against K033243: 6 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K151798Inclusive Titanium Abutments compatible with: Straumann synOcta Implant SystemPrismatik Dentalcraft, Inc.20150

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 6 companies; a new generation was cleared every 1.6 years on median.
  • 11 of the 70 ancestors have a recall of any class.
  • Of its descendants, K151798 (Prismatik Dentalcraft, Inc., 2015) has gone furthest, with 0 descendants of its own.
  • 6 other devices also cite its predicate K033243.

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. 2014, 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?

Inclusive Titanium Abutments are premanufactured prosthetic components directly connected to endosseous dental implants and are intended for use as an aid in prosthetic rehabilitation.

Inclusive Titanium Abutments are compatible with Straumann Standard Plus Tissue Level Implants in RN (4.1 mm and 4.8 mm) and WN (4.8 mm) sizes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141211: Inclusive Titanium Abutments Compatible with Straumann Tissue Level Implants.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141211

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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