510(k) Report

510(k) · Cleared

Cleared

Osseotite NT Dental Implants & Accessories

K014235510(k) TraditionalCleared May 16, 2002141-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

Implant Innovations, Inc. · DZE Implant, Endosseous, Root-Form

Cleared on May 16, 2002 as substantially equivalent to K935544 (Implant Innovations International, Inc., 1995) and 4 other predicates after a 141-day review. Its family tree reaches back 2 generations to 1993. 583 later devices descend from it.

Decided
May 16, 2002
Review
141 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
5

Its longest line of descent runs back 2 generations to K925765 (1993). 6 ancestors in all. 583 later devices descend from it, 11 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor1995: 1 other ancestor2007: 18 descendants cleared2003: 4 descendants cleared2005: 5 descendants cleared2004: 3 descendants cleared2002: 1 descendant cleared2008: 12 descendants cleared2006: 3 descendants cleared2010: 5 descendants cleared2013: 23 descendants cleared2011: 16 descendants cleared2015: 31 descendants cleared2018: 31 descendants cleared2014: 20 descendants cleared2012: 16 descendants cleared2017: 29 descendants cleared2009: 7 descendants cleared2019: 27 descendants cleared2016: 31 descendants cleared2021: 41 descendants cleared2022: 42 descendants cleared2024: 57 descendants cleared2025: 47 descendants cleared2026: 26 descendants cleared2020: 41 descendants cleared2023: 47 descendants clearedK925765 · Branemark System Standard 3.75MM Fixture · Nobelpharma USA, Inc. · 1993K994376 · Frialit-2 3.4MM Steeped Cylinder Implant with Frios TPS Coating; Frialit-2 3.4MM Steeped Cylinder Implant with Frios HA · Friadent GmbH · 20001990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 4 other ancestors 1 generation forward: 11 descendants2 generations forward: 29 descendants3 generations forward: 101 descendants4 generations forward: 147 descendants5 generations forward: 100 descendants6 generations forward: 74 descendants7 generations forward: 67 descendants8 generations forward: 32 descendants9 generations forward: 12 descendants10 generations forward: 4 descendants11 generations forward: 3 descendants12 generations forward: 3 descendants K994376 · Frialit-2 3.4MM Steeped Cylinder Implant with Frios TPS Coating; Frialit-2 3.4MM Steeped Cylinder Implant with Frios HA · Friadent GmbH · 2000K925765 · Branemark System Standard 3.75MM Fixture · Nobelpharma USA, Inc. · 19930+5+10
  1. Root · 2 generations backK925765 Branemark System Standard 3.75MM FixtureNobelpharma USA, Inc. · 1993
  2. 1 generation backK994376 Frialit-2 3.4MM Steeped Cylinder Implant with Frios TPS Coating…Friadent GmbH · 2000
  3. This deviceK014235 Osseotite NT Dental Implants & AccessoriesImplant Innovations, Inc. · 2002
  4. Descendant · cites it directly · 478 of its ownK022009 3I Implants; Osseotite Dental Implants; Osseotite NT Dental ImplantsImplant Innovations, Inc. · 2002
  5. Descendant · cites it directly · 361 of its ownK062069 Atlantis Abutment for 3I Micromini ImplantAtlantis Components, Inc. · 2007
  6. Descendant · 2 generations on · 357 of its ownK070833 Atlantis Abutment for Astra ImplantAtlantis Components, Inc. · 2007
  7. Descendant · 3 generations on · 337 of its ownK081666 Atlantis, Atlantis Gemini, Atlantis Gemini+ Abutments for Astra…Astra Tech, Inc. · 2008
  8. Descendant · cites it directly · 330 of its ownK031475 Osseotite NT Certain ImplantsImplant Innovations, Inc. · 2003

Showing 5 of 583 descendants. See all descendants

Descendants cleared per year

2002: 12003: 42004: 32005: 52006: 32007: 182008: 122009: 72010: 52011: 162012: 162013: 232014: 202015: 312016: 312017: 292018: 312019: 272020: 412021: 412022: 422023: 472024: 572025: 472026: 26
2002high 57 (2024) · low 1 (2002)2026

Most influential descendants

Showing 5 of 583 · See all
  • K0220093I Implants; Osseotite Dental Implants; Osseotite NT Dental ImplantsImplant Innovations, Inc. · 2002 · cites it directly478descendants
  • K062069Atlantis Abutment for 3I Micromini ImplantAtlantis Components, Inc. · 2007 · cites it directly361descendants
  • K070833Atlantis Abutment for Astra ImplantAtlantis Components, Inc. · 2007 · 2 generations on357descendants
  • K081666Atlantis, Atlantis Gemini, Atlantis Gemini+ Abutments for Astra Osseospeed 3.0 ImplantsAstra Tech, Inc. · 2008 · 3 generations on337descendants
  • K031475Osseotite NT Certain ImplantsImplant Innovations, Inc. · 2003 · cites it directly330descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K925765Branemark System Standard 3.75MM FixtureNobelpharma USA, Inc.1993—
−1K994376Frialit-2 3.4MM Steeped Cylinder Implant with Frios TPS Coating; Frialit-2…Friadent GmbH2000—
0 (this device)K014235Osseotite NT Dental Implants & AccessoriesImplant Innovations, Inc.2002—
+1K0220093I Implants; Osseotite Dental Implants; Osseotite NT Dental ImplantsImplant Innovations, Inc.2002—
+1K062069Atlantis Abutment for 3I Micromini ImplantAtlantis Components, Inc.2007—
+2K070833Atlantis Abutment for Astra ImplantAtlantis Components, Inc.2007—
+3K081666Atlantis, Atlantis Gemini, Atlantis Gemini+ Abutments for Astra Osseospeed 3.0…Astra Tech, Inc.2008—
+1K031475Osseotite NT Certain ImplantsImplant Innovations, Inc.2003—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199810
199910
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200340
200430
200550
200630
2007180
2008120
200970
201050
2011160
2012160
2013230
2014200
2015310
2016310
2017290
2018310
2019270
2020410
2021410
2022420
2023470
2024570
2025470
2026260
FIG. 1 — Lineage of K014235, 1993–2026Source: 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 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? (6)

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
*K9355443I Standard Threaded/Self-Tapping Threaded Implants Modification
Summary page 1
…III Common Name: Endosseous Implant PREDICATE DEVICES: OSSEOTITE® Dental Implants and Accessories cleared for marketing via the following premarket notifications: e K935544 for an acid-etched process to create the OSSEOTITE® Brand surface cleared on March 13, 1995, e K980549 for a performance claim…
Implant Innovations International, Inc.1995—
*K980549Osseotite Dental Implant System
Summary page 1
…red for marketing via the following premarket notifications: e K935544 for an acid-etched process to create the OSSEOTITE® Brand surface cleared on March 13, 1995, e K980549 for a performance claim cleared on April 28, 1998, o K983347 for a performance claim cleared on January 1, 1999, and ¢ XO013570…
Implant Innovations, Inc.1998—
*K983347Osseotite Dental Implants
Summary page 1
…e K935544 for an acid-etched process to create the OSSEOTITE® Brand surface cleared on March 13, 1995, e K980549 for a performance claim cleared on April 28, 1998, o K983347 for a performance claim cleared on January 1, 1999, and ¢ XO013570 for Instructions for Use changes cleared on December 18, 2001.…
Implant Innovations, Inc.1999—
*K002475Replace TPS Coated Implants
Summary page 1
…eature is substantially equivalent to at least two currently marketed dental implants: ¢ Nobel Biocare USA, Inc. (Steri-Oss), Replace™ TPS Coated Implants cleared via K002475 on November 9, 2000, and the e Friadent GmbH FRIALITT™-2 Stepped Screw Implant cleared via K994376 on March 24, 2000. December…
Nobel Biocare Uas, Inc.2000—
*K994376Frialit-2 3.4MM Steeped Cylinder Implant with Frios TPS Coating; Frialit-2 3.4MM Steeped…
Summary page 1
…care USA, Inc. (Steri-Oss), Replace™ TPS Coated Implants cleared via K002475 on November 9, 2000, and the e Friadent GmbH FRIALITT™-2 Stepped Screw Implant cleared via K994376 on March 24, 2000. December 21, 2001 Implant Innovations, Inc. 510(k) Premarket Notification OSSEOTITE NT™ Impl…
Friadent GmbH2000—
*—OSSEOTITE® Dental Implants and Accessories
Named without a submission number
—

Also cleared against K935544: 12 other devices →

What descends from it? (583)

See all 583

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

NumberDeviceApplicantDecidedDescendants
K0220093I Implants; Osseotite Dental Implants; Osseotite NT Dental ImplantsImplant Innovations, Inc.2002478
K062069Atlantis Abutment for 3I Micromini ImplantAtlantis Components, Inc.2007361
K031475Osseotite NT Certain ImplantsImplant Innovations, Inc.2003330
K031632Osseotite Iol Implants and Osseotite Certain Iol ImplantsImplant Innovations, Inc.2003320
K0306143I Dental ImplantsImplant Innovations, Inc.2003319
K041402Modification to Osseotite NT Certain ImplantsImplant Innovations, Inc.2004318
K0514613I Osseotite Dental ImplantsImplant Innovations, Inc.2005312
K063286Osseotite; Osseotite NT; XP; TG OsseotiteImplant Innovations, Inc.2007211
K072483Atlantis Abutment in Zirconia for 3I Certain Microamini Implants, Gemini Abutment in…Atlantis Components, Inc.200728
K062636Osseotite, Osseotite NY, Certain, Certain NT, Prevail, Certain Prevail, XP…Implant Innovations, Inc.200728

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 9 years and passes through 3 companies; a new generation was cleared every 6.5 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K022009 (Implant Innovations, Inc., 2002) has gone furthest, with 478 descendants of its own.
  • 12 other devices also cite its predicate K935544.

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.

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?

OSSEOTITE NT™ Implant System is indicated for surgical placement in the upper or lower jaw to provide a means for prosthetic attachment to restore a patient’s chewing function.

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. “K014235: Osseotite NT Dental Implants & Accessories.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K014235

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026