510(k) Report

510(k) · Cleared

Cleared

P.004 Abutments

K072679510(k) SpecialCleared Oct 12, 200721-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

Institut Straumann AG · NHA Abutment, Implant, Dental, Endosseous

Cleared on Oct 12, 2007 as substantially equivalent to K062129 (Institut Straumann AG, 2006) and 1 other predicate after a 21-day review. Its family tree reaches back 7 generations to 1990. 279 later devices descend from it.

Decided
Oct 12, 2007
Review
21 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K894844 (1990). 16 ancestors in all. 279 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2001: 2 other ancestors2004: 1 other ancestor1996: 1 other ancestor2002: 1 other ancestor1995: 1 other ancestor1993: 1 other ancestor1992: 1 other ancestor2013: 4 descendants cleared2012: 3 descendants cleared2009: 1 descendant cleared2017: 15 descendants cleared2011: 2 descendants cleared2024: 42 descendants cleared2014: 5 descendants cleared2015: 10 descendants cleared2020: 23 descendants cleared2023: 40 descendants cleared2021: 26 descendants cleared2016: 11 descendants cleared2019: 13 descendants cleared2022: 20 descendants cleared2026: 19 descendants cleared2025: 29 descendants cleared2018: 16 descendants clearedK894844 · Bonefit Implant System Accessories & Instruments · Straumann Institute, Ltd. · 1990K990342 · Synocta Prosthetics · Straumann USA · 1999×2: 2 generations cleared close together, K013798 (2001), K020096 (2002) K033243 · Iti Synocta Meso Abutments · Straumann USA · 2003K062129 · P.0004 Implants · Institut Straumann AG · 2006K070478 · P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap) · Straumann Manufacturing, Inc. · 20071990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors3 generations back: 3 other ancestors4 generations back: 4 other ancestors 1 generation forward: 4 descendants2 generations forward: 14 descendants3 generations forward: 46 descendants4 generations forward: 41 descendants5 generations forward: 52 descendants6 generations forward: 50 descendants7 generations forward: 32 descendants8 generations forward: 18 descendants9 generations forward: 10 descendants10 generations forward: 7 descendants11 generations forward: 4 descendants12 generations forward: 1 descendant K070478 · P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap) · Straumann Manufacturing, Inc. · 2007K062129 · P.0004 Implants · Institut Straumann AG · 2006K033243 · Iti Synocta Meso Abutments · Straumann USA · 2003K020096 · Esthetic Ease Abutments for the Iti Dental Implant System · Institut Straumann AG · 2002 · recalledK013798 · Prosthetic Accessories to the Iti Dental Implant System · Institut Straumann AG · 2001K990342 · Synocta Prosthetics · Straumann USA · 1999K894844 · Bonefit Implant System Accessories & Instruments · Straumann Institute, Ltd. · 1990−50+5+10
  1. Root · 7 generations backK894844 Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd. · 1990
  2. 6 generations backK990342 Synocta ProstheticsStraumann USA · 1999
  3. 5 generations backK013798 Prosthetic Accessories to the Iti Dental Implant SystemInstitut Straumann AG · 2001
  4. 4 generations backK020096 Esthetic Ease Abutments for the Iti Dental Implant SystemInstitut Straumann AG · 2002 · Recalled
  5. 3 generations backK033243 Iti Synocta Meso AbutmentsStraumann USA · 2003
  6. 2 generations backK062129 P.0004 ImplantsInstitut Straumann AG · 2006
  7. 1 generation backK070478 P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap)Straumann Manufacturing, Inc. · 2007
  8. This deviceK072679 P.004 AbutmentsInstitut Straumann AG · 2007
  9. Descendant · cites it directly · 223 of its ownK092814 Straumann Dental AbutmentsStraumann Manufacturing, Inc. · 2009
  10. Descendant · 2 generations on · 222 of its ownK111357 Straumann Narrow Neck Crossfit (NNC) 03.3MM Dental Implant SystemStraumann USA · 2011
  11. Descendant · 3 generations on · 166 of its ownK113283 NNC Cementable Abutment Straight,15 Degree Angle, Type a ,15 Degree…Straumann USA · 2011
  12. Descendant · 4 generations on · 165 of its ownK120822 Straumann Cares Variobase Abutment NNC, Straumann Cares Variobase…Institut Straumann AG · 2012
  13. Descendant · 5 generations on · 129 of its ownK150203 Medentika CAD/CAM AbutmentsMedentika GmbH · 2015

Showing 5 of 279 descendants. See all descendants

Descendants cleared per year

2009: 12011: 22012: 32013: 42014: 52015: 102016: 112017: 152018: 162019: 132020: 232021: 262022: 202023: 402024: 422025: 292026: 19
2009high 42 (2024) · low 0 (2010)2026

Most influential descendants

Showing 5 of 279 · See all
  • K092814Straumann Dental AbutmentsStraumann Manufacturing, Inc. · 2009 · cites it directly223descendants
  • K111357Straumann Narrow Neck Crossfit (NNC) 03.3MM Dental Implant SystemStraumann USA · 2011 · 2 generations on222descendants
  • K113283NNC Cementable Abutment Straight,15 Degree Angle, Type a ,15 Degree Angle, Type B,NNC…Straumann USA · 2011 · 3 generations on166descendants
  • K120822Straumann Cares Variobase Abutment NNC, Straumann Cares Variobase Abutment RN, Straumann…Institut Straumann AG · 2012 · 4 generations on165descendants
  • K150203Medentika CAD/CAM AbutmentsMedentika GmbH · 2015 · 5 generations on129descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K894844Bonefit Implant System Accessories & InstrumentsStraumann Institute, Ltd.1990—
−6K990342Synocta ProstheticsStraumann USA1999—
−5K013798Prosthetic Accessories to the Iti Dental Implant SystemInstitut Straumann AG2001—
−4K020096Esthetic Ease Abutments for the Iti Dental Implant SystemInstitut Straumann AG20021
−3K033243Iti Synocta Meso AbutmentsStraumann USA2003—
−2K062129P.0004 ImplantsInstitut Straumann AG2006—
−1K070478P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap)Straumann Manufacturing, Inc.2007—
0 (this device)K072679P.004 AbutmentsInstitut Straumann AG2007—
+1K092814Straumann Dental AbutmentsStraumann Manufacturing, Inc.2009—
+2K111357Straumann Narrow Neck Crossfit (NNC) 03.3MM Dental Implant SystemStraumann USA2011—
+3K113283NNC Cementable Abutment Straight,15 Degree Angle, Type a ,15 Degree Angle…Straumann USA2011—
+4K120822Straumann Cares Variobase Abutment NNC, Straumann Cares Variobase Abutment RN…Institut Straumann AG2012—
+5K150203Medentika CAD/CAM AbutmentsMedentika GmbH2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199310
199510
199610
200120
200210
200410
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201120
201230
201340
201450
2015100
2016110
2017150
2018160
2019130
2020230
2021260
2022200
2023400
2024420
2025290
2026190
FIG. 1 — Lineage of K072679, 1990–2026Source: 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 30.7 · 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
*K062129P.0004 Implants
Summary page 1
…ber: §872.3630 3. Legally Marketed Device to which Equivalence is Claimed (Predicate Device) Straumann P.004 Dental Implants, K062129 P.004 RC Temporary Abutments, K070478 4. Description of the Device The Straumann P.004 Dental Implant Sy…
Institut Straumann AG2006—
*K070478P.004 RC Temporary Abutment, P.004 Temporary Healing Abutment (Cap)
Summary page 1
…ally Marketed Device to which Equivalence is Claimed (Predicate Device) Straumann P.004 Dental Implants, K062129 P.004 RC Temporary Abutments, K070478 4. Description of the Device The Straumann P.004 Dental Implant System is an integrated system of endlos…
Straumann Manufacturing, Inc.2007—

Also cleared against K062129: 30 other devices →

What descends from it? (279)

See all 279

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K092814Straumann Dental AbutmentsStraumann Manufacturing, Inc.2009223
K121585TS Implant SystemOsstem Implant Co., Ltd.201364
K130808Straumann Healing Abutments, Healing Caps, Closure ScrewsStraumann USA201339
K122192NC Temporary Abutment, Cad-Temp, Pmma RC Temporary Abutment, Cad-Temp, Pmma RN Temporary…Straumann USA, LLC20121

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 17 years and passes through 4 companies; a new generation was cleared every 1.7 years on median.
  • 1 of the 16 ancestors has a recall of any class.
  • Of its descendants, K092814 (Straumann Manufacturing, Inc., 2009) has gone furthest, with 223 descendants of its own.
  • 30 other devices also cite its predicate K062129.

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. 2007, 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?

P.004 NC Temporary Abutment is indicated for use in Straumann P.004 NC Bone Level implants for temporary restorations of single crowns and bridges for up to six months.

P.004 NC Healing Abutment, customizable is indicated for use in Straumann P.004 NC Bone Level implants to protect the inner configuration of the implant and maintains, stabilizes and forms the soft tissue during the healing process for up to six months and should be placed out of occlusion.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072679: P.004 Abutments.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K072679

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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