510(k) Report

510(k) · Cleared

Cleared

TL 04.1MM RN,S, Slactive Tizr 6, 8, 10, 12, 14, 16MM Dental Implants

K122855510(k) TraditionalCleared Dec 12, 201285-day reviewClass II21 CFR 872.3640

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

Straumann USA · DZE Implant, Endosseous, Root-Form

Cleared on Dec 12, 2012 as substantially equivalent to K983742 (Institut Straumann AG, 1999) and 8 other predicates after an 85-day review. Its family tree reaches back 9 generations to 1990. 123 later devices descend from it.

Decided
Dec 12, 2012
Review
85 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
9

Its longest line of descent runs back 9 generations to K894595 (1990). 43 ancestors in all, the oldest K894844 (1990). 123 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2004: 1 other ancestor2001: 5 other ancestors1999: 2 other ancestors2006: 1 other ancestor2003: 5 other ancestors1997: 1 other ancestor1996: 5 other ancestors1990: 2 other ancestors2002: 3 other ancestors2000: 1 other ancestor1998: 2 other ancestors1995: 1 other ancestor1994: 2 other ancestors1993: 2 other ancestors2013: 2 descendants cleared2014: 1 descendant cleared2015: 4 descendants cleared2022: 12 descendants cleared2018: 4 descendants cleared2024: 17 descendants cleared2021: 9 descendants cleared2017: 4 descendants cleared2016: 1 descendant cleared2019: 7 descendants cleared2025: 24 descendants cleared2026: 13 descendants cleared2023: 17 descendants cleared2020: 8 descendants clearedK894595 · Bonefit R Screw Implants · Institut Straumann AG · 1990K984104 · Iti Dental Implant System · Straumann USA · 1999 · recalledK992937 · Dental Implant · Nobel Biocare Uas, Inc. · 2000 · recalled×2: 2 generations cleared close together, K013067 (2002), K021318 (2002) K032158 · Xive Dental Implant System Multiple · Friadent GmbH · 2003K033984 · Straumann Dental Implant System · Institut Straumann AG · 2004K053088 · Slactive Implants · Institut Straumann AG · 2006K081419 · Straumann Dental Implant System · Institut Straumann AG · 20091990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 6 other ancestors2 generations back: 12 other ancestors3 generations back: 13 other ancestors4 generations back: 1 other ancestor5 generations back: 2 other ancestors 1 generation forward: 2 descendants2 generations forward: 11 descendants3 generations forward: 28 descendants4 generations forward: 31 descendants5 generations forward: 26 descendants6 generations forward: 11 descendants7 generations forward: 9 descendants8 generations forward: 4 descendants9 generations forward: 1 descendant K081419 · Straumann Dental Implant System · Institut Straumann AG · 2009K053088 · Slactive Implants · Institut Straumann AG · 2006K033984 · Straumann Dental Implant System · Institut Straumann AG · 2004K032158 · Xive Dental Implant System Multiple · Friadent GmbH · 2003K021318 · Xive Dental Implant System · Friadent GmbH · 2002K013067 · Frialoc Dental Implant System · Friadent GmbH · 2002K992937 · Dental Implant · Nobel Biocare Uas, Inc. · 2000 · recalledK984104 · Iti Dental Implant System · Straumann USA · 1999 · recalledK894595 · Bonefit R Screw Implants · Institut Straumann AG · 1990−50+5
  1. Root · 9 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 5 generations between
  3. 3 generations backK033984 Straumann Dental Implant SystemInstitut Straumann AG · 2004
  4. 2 generations backK053088 Slactive ImplantsInstitut Straumann AG · 2006
  5. 1 generation backK081419 Straumann Dental Implant SystemInstitut Straumann AG · 2009
  6. This deviceK122855 TL 04.1MM RN,S, Slactive Tizr 6, 8, 10, 12, 14, 16MM Dental ImplantsStraumann USA · 2012
  7. Descendant · cites it directly · 122 of its ownK123784 Straumann Dental Implant SystemStraumann USA, LLC · 2013
  8. Descendant · cites it directly · 118 of its ownK130222 Straumann Dental Implant SystemStraumann USA, LLC · 2013
  9. Descendant · 2 generations on · 105 of its ownK140878 Straumann Bone Level Tapered ImplantStraumann USA, LLC · 2014 · Recalled
  10. Descendant · 2 generations on · 86 of its ownK170588 DESS Dental Smart SolutionsTerrats Medical SL · 2017
  11. Descendant · 2 generations on · 51 of its ownK173908 DESS Dental Smart SolutionsTerrats Medical SL · 2018
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 backK992937 Dental ImplantNobel Biocare Uas, Inc. · 2000 · Recalled
  4. 6 generations backK013067 Frialoc Dental Implant SystemFriadent GmbH · 2002
  5. 5 generations backK021318 Xive Dental Implant SystemFriadent GmbH · 2002
  6. 4 generations backK032158 Xive Dental Implant System MultipleFriadent GmbH · 2003
  7. 3 generations backK033984 Straumann Dental Implant SystemInstitut Straumann AG · 2004
  8. 2 generations backK053088 Slactive ImplantsInstitut Straumann AG · 2006
  9. 1 generation backK081419 Straumann Dental Implant SystemInstitut Straumann AG · 2009
  10. This deviceK122855 TL 04.1MM RN,S, Slactive Tizr 6, 8, 10, 12, 14, 16MM Dental ImplantsStraumann USA · 2012

Showing 5 of 123 descendants. See all descendants

Descendants cleared per year

2013: 22014: 12015: 42016: 12017: 42018: 42019: 72020: 82021: 92022: 122023: 172024: 172025: 242026: 13
2013high 24 (2025) · low 1 (2014)2026

Most influential descendants

Showing 5 of 123 · See all
  • K123784Straumann Dental Implant SystemStraumann USA, LLC · 2013 · cites it directly122descendants
  • K130222Straumann Dental Implant SystemStraumann USA, LLC · 2013 · cites it directly118descendants
  • K140878Straumann Bone Level Tapered ImplantStraumann USA, LLC · 2014 · 2 generations on105descendants
  • K170588DESS Dental Smart SolutionsTerrats Medical SL · 2017 · 2 generations on86descendants
  • K173908DESS Dental Smart SolutionsTerrats Medical SL · 2018 · 2 generations on51descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−8K984104Iti Dental Implant SystemStraumann USA19991
−7K992937Dental ImplantNobel Biocare Uas, Inc.20001
−6K013067Frialoc Dental Implant SystemFriadent GmbH2002—
−5K021318Xive Dental Implant SystemFriadent GmbH2002—
−4K032158Xive Dental Implant System MultipleFriadent GmbH2003—
−3K033984Straumann Dental Implant SystemInstitut Straumann AG2004—
−2K053088Slactive ImplantsInstitut Straumann AG2006—
−1K081419Straumann Dental Implant SystemInstitut Straumann AG2009—
0 (this device)K122855TL 04.1MM RN,S, Slactive Tizr 6, 8, 10, 12, 14, 16MM Dental ImplantsStraumann USA2012—
+1K123784Straumann Dental Implant SystemStraumann USA, LLC2013—
+1K130222Straumann Dental Implant SystemStraumann USA, LLC2013—
+2K140878Straumann Bone Level Tapered ImplantStraumann USA, LLC20142
+2K170588DESS Dental Smart SolutionsTerrats Medical SL2017—
+2K173908DESS Dental Smart SolutionsTerrats Medical SL2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199020
199320
199420
199510
199650
199710
199820
199920
200010
200150
200230
200350
200410
200610
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201320
201410
201540
201610
201740
201840
201970
202080
202190
2022120
2023170
2024170
2025240
2026130
FIG. 1 — Lineage of K122855, 1990–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 DZE? 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 DZE device

  1. #1 K211090 ZENEX Implant Systemscore 25.4 · 15 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? (9)

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
*K983742Iti Dental Implant System
Summary page 1
…nt, Endosseous, Root-form Regulation Number: §872.3640 4. Legally Marketed Device to which Equivalence is Claimed (Predicate Device) K983742, ITI All-in-One Implant K003552, ITI Dental Implant System Modification K033922, ITI Dental Implant System K…
Institut Straumann AG1999—
*K003552Iti Dental Implant System
Summary page 1
…tion Number: §872.3640 4. Legally Marketed Device to which Equivalence is Claimed (Predicate Device) K983742, ITI All-in-One Implant K003552, ITI Dental Implant System Modification K033922, ITI Dental Implant System K003271, ITI Dental Implants K012…
Institut Straumann SA2001—
*K033922Modification to Iti Dental Implant System
Summary page 1
…ted Device to which Equivalence is Claimed (Predicate Device) K983742, ITI All-in-One Implant K003552, ITI Dental Implant System Modification K033922, ITI Dental Implant System K003271, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental…
Institut Straumann AG20041
*K003271Modification to Iti Dental Implant System
Summary page 1
…(Predicate Device) K983742, ITI All-in-One Implant K003552, ITI Dental Implant System Modification K033922, ITI Dental Implant System K003271, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental Implant System Modification, SLActive…
Institut Straumann AG2001—
*K012757Iti Dental Implant System
Summary page 1
…83742, ITI All-in-One Implant K003552, ITI Dental Implant System Modification K033922, ITI Dental Implant System K003271, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental Implant System Modification, SLActive K053088, SLActive New Claims…
Straumann USA2001—
*K033984Straumann Dental Implant System
Summary page 1
…2, ITI Dental Implant System Modification K033922, ITI Dental Implant System K003271, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental Implant System Modification, SLActive K053088, SLActive New Claims K081419, Modified TE 3.3 RN Implant…
Institut Straumann AG2004—
*K053088Slactive Implants
Summary page 1
…Dental Implant System K003271, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental Implant System Modification, SLActive K053088, SLActive New Claims K081419, Modified TE 3.3 RN Implant K083550, Modified Straumann Dental Implants 5. Descrip…
Institut Straumann AG2006—
*K081419Straumann Dental Implant System
Summary page 1
…1, ITI Dental Implants K012757, ITI Tapered Dental Implant K033984, Dental Implant System Modification, SLActive K053088, SLActive New Claims K081419, Modified TE 3.3 RN Implant K083550, Modified Straumann Dental Implants 5. Description of the Device The propos…
Institut Straumann AG2009—
*K083550Straumann Dental Implant System
Summary page 1
…Tapered Dental Implant K033984, Dental Implant System Modification, SLActive K053088, SLActive New Claims K081419, Modified TE 3.3 RN Implant K083550, Modified Straumann Dental Implants 5. Description of the Device The proposed Straumann Tissue Level 04.1 mm and 04.8…
Straumann USA2009—

Also cleared against K983742: 6 other devices →

What descends from it? (123)

See all 123

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

NumberDeviceApplicantDecidedDescendants
K123784Straumann Dental Implant SystemStraumann USA, LLC2013122
K130222Straumann Dental Implant SystemStraumann USA, LLC2013118

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 22 years and passes through 4 companies; a new generation was cleared every 1.7 years on median.
  • 4 of the 43 ancestors have a recall of any class.
  • Of its descendants, K123784 (Straumann USA, LLC, 2013) has gone furthest, with 122 descendants of its own.
  • 6 other devices also cite its predicate K983742.

How does its category compare?

All DZE devices

DZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · DZE

31in 2025

2007: 432008: 612009: 412010: 342011: 262012: 392013: 422014: 362015: 362016: 402017: 482018: 412019: 312020: 412021: 342022: 342023: 352024: 402025: 312026 (partial year): 15
2007high 61 (2008) · low 26 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DZE

184in 2025

2007: 107 days median2008: 118 days median2009: 110 days median2010: 162 days median2011: 194 days median2012: 174 days median2013: 195 days median2014: 265 days median2015: 215 days median2016: 219 days median2017: 223 days median2018: 200 days median2019: 231 days median2020: 230 days median2021: 182 days median2022: 243 days median2023: 248 days median2024: 222 days median2025: 184 days median2026 (partial year): 194 days median
2007high 265 (2014) · low 107 (2007)2026

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

Recalls per year · DZE

1in 2025

2007: 112008: 42009: 32010: 32012: 112013: 12014: 72015: 32016: 152017: 42018: 42019: 82021: 62024: 12025: 12026 (partial year): 2
2007high 15 (2016) · low 0 (2011)2026

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

Adverse event reports per year · DZE

465,788in 2025

2007: 2252008: 3932009: 1642010: 3602011: 3622012: 3582013: 3912014: 1,1242015: 2,8942016: 1,1162017: 9,7192018: 12,8922019: 167,0162020: 255,5242021: 479,6182022: 483,2242023: 537,5852024: 473,6292025: 465,788
2007high 537,585 (2023) · low 164 (2009)2025

MAUDE reports naming product code DZE, 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
20074310711225
2008611184393
2009411103164
2010341623360
2011261940362
20123917411358
2013421951391
20143626571,124
20153621532,894
201640219151,116
20174822349,719
201841200412,892
2019312318167,016
2020412300255,524
2021341826479,618
2022342430483,224
2023352480537,585
2024402221473,629
2025311841465,788
2026151942—

What is it indicated for?

Straumnanno dental implants are suitable for the treatment of oral endosteal implantation in the upper and lower jaw and for the functional and esthetic oral rehabilitation of edentulous and partially dentate patients (unless specific indications and limitations are present, as stated below). Straumanne dental Implants can also be used for Immediate or early, Implantation following extraction or loss of natural teeth. Implants can be placed with…

Read the full statement (143 words)

Straumnanno dental implants are suitable for the treatment of oral endosteal implantation in the upper and lower jaw and for the functional and esthetic oral rehabilitation of edentulous and partially dentate patients (unless specific indications and limitations are present, as stated below). Straumanne dental Implants can also be used for Immediate or early, Implantation following extraction or loss of natural teeth. Implants can be placed with immediate function on single-tooth and/or multiple tooth applications when good primary stability is achieved and with appropriate occlusal loading, to restore chewing function. The prosthetic restorations used are single crowns, bridges and partial or full dentures, which are connected to the Implants by the corresponding elements (abutments). When placing implants in the posterior region, we recommend using only large diameter implants. Incases of fully edentulous patients, 4 or more implants must be used in immediately loaded cases.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122855: TL 04.1MM RN,S, Slactive Tizr 6, 8, 10, 12, 14, 16MM Dental Implants.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122855

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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