510(k) Report

510(k) · Cleared

Cleared

NUVENTUS NV.C™ Dental Implant System

K233081510(k) TraditionalCleared Nov 15, 2024416-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

Infinitum Eta, Ltd. · DZE Implant, Endosseous, Root-Form

Cleared on Nov 15, 2024 as substantially equivalent to K142260 (Nobel Biocare AB, 2015) after a 416-day review. Its family tree reaches back 11 generations to 1990.

Decided
Nov 15, 2024
Review
416 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K894595 (1990). 87 ancestors in all, the oldest K871863 (1987). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2010: 1 other ancestor2013: 1 other ancestor2009: 2 other ancestors2005: 3 other ancestors2006: 1 other ancestor2004: 5 other ancestors1994: 10 other ancestors2003: 2 other ancestors2002: 4 other ancestors1998: 4 other ancestors1996: 10 other ancestors2001: 4 other ancestors1999: 3 other ancestors1997: 4 other ancestors1989: 2 other ancestors1987: 1 other ancestor1995: 7 other ancestors1993: 10 other ancestors1991: 1 other ancestor1990: 1 other ancestorReference device: K163349 · MIS V3 Conical Connection Dental Implant System­ · Mis Implants Technologies, Ltd. · 2017Reference device: K181850 · Inversa Implants · Southern Implants (Pty), Ltd. · 2018Reference device: K071370 · Nobelactive Internal Connection Implant · Nobel Biocare AB · 2007 · recalledReference device: K161435 · Temporary Snap Abutment · Nobel Biocare AB · 2016 · recalledReference device: K161416 · Multi-unit Abutment Plus · Nobel Biocare AB · 2017K894595 · 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 · recalledK083205 · Nobelactive 8.5 MM & 18.0 MM · Nobel Biocare AB · 2009K133731 · Nobelactive Wide Platform (WP) · Nobel Biocare AB · 2014K142260 · NobelActive · Nobel Biocare AB · 20151990200020102020
  1. Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 7 generations between
  3. 3 generations backK083205 Nobelactive 8.5 MM & 18.0 MMNobel Biocare AB · 2009
  4. 2 generations backK133731 Nobelactive Wide Platform (WP)Nobel Biocare AB · 2014
  5. 1 generation backK142260 NobelActiveNobel Biocare AB · 2015
  6. This deviceK233081 NUVENTUS NV.C™ Dental Implant SystemInfinitum Eta, Ltd. · 2024
Show all 11 generations
  1. Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 10 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 9 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 8 generations backK023113 Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc. · 2002 · Recalled
  5. 7 generations backK041661 Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc. · 2004
  6. 6 generations backK050258 Groovy ImplantsNobel Biocare AB · 2005 · Recalled
  7. 5 generations backK061003 SFB & CFB ImplantsNobel Biocare AB · 2006
  8. 4 generations backK071370 Nobelactive Internal Connection ImplantNobel Biocare AB · 2007 · Recalled
  9. 3 generations backK083205 Nobelactive 8.5 MM & 18.0 MMNobel Biocare AB · 2009
  10. 2 generations backK133731 Nobelactive Wide Platform (WP)Nobel Biocare AB · 2014
  11. 1 generation backK142260 NobelActiveNobel Biocare AB · 2015
  12. This deviceK233081 NUVENTUS NV.C™ Dental Implant SystemInfinitum Eta, Ltd. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−10K984104Iti Dental Implant SystemStraumann USA19991
−9K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−8K023113Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc.200227
−7K041661Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc.2004—
−6K050258Groovy ImplantsNobel Biocare AB200528
−5K061003SFB & CFB ImplantsNobel Biocare AB2006—
−4K071370Nobelactive Internal Connection ImplantNobel Biocare AB20074
−3K083205Nobelactive 8.5 MM & 18.0 MMNobel Biocare AB2009—
−2K133731Nobelactive Wide Platform (WP)Nobel Biocare AB2014—
−1K142260NobelActiveNobel Biocare AB2015—
0 (this device)K233081NUVENTUS NV.C™ Dental Implant SystemInfinitum Eta, Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198920
199010
199110
1993100
1994100
199570
1996100
199740
199840
199930
200140
200240
200320
200450
200530
200610
200920
201010
201310
FIG. 1 — Lineage of K233081, 1990–2024Source: 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? (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
*K142260NobelActive
Summary page 5
…almic, Anesthesia, Respiratory, ENT and Dental Devices) Reviewing Division Division of Dental and ENT Devices PREDICATE DEVICE INFORMATION Primary Predicate Device K142260, NobelActive®, Nobel Biocare AB Reference Devices K163349, MIS V3 Conical Connection Dental Implant System, MIS Implants Technol…
Nobel Biocare AB2015—
†K163349MIS V3 Conical Connection Dental Implant System­Mis Implants Technologies, Ltd.2017—
†K181850Inversa ImplantsSouthern Implants (Pty), Ltd.2018—
†K071370Nobelactive Internal Connection ImplantNobel Biocare AB20074
†K161435Temporary Snap AbutmentNobel Biocare AB20161
†K161416Multi-unit Abutment PlusNobel Biocare AB2017—

Also cleared against K142260: 9 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 34 years and passes through 5 companies; a new generation was cleared every 1.5 years on median.
  • 11 of the 87 ancestors have a recall of any class.
  • 9 other devices also cite its predicate K142260.

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. 2024, 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?

NUVENTUS NV.C™ Dental Implants are indicated for the functional and esthetic oral rehabilitation of the upper or lower jaw of edentulous or partially edentulous patients. NUVENTUS NV.C™ dental implants may be used for immediate, early or delayed implantation following the extraction or loss of natural teeth. The implants can be placed with immediate loading for single-tooth or multiple teeth restorations when good primary stability is achieved and with appropriate occlusal loading to restore chewing function. NUVENTUS NV.C™ Dental Implants are compatible for use with the following prosthetic interfaces.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K233081: NUVENTUS NV.C™ Dental Implant System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K233081

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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