510(k) Report

510(k) · Cleared

Cleared

Alpha Dent Implants Dental Implants System

K210499510(k) TraditionalCleared Nov 1, 2021252-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

Alpha Dent Implants GmbH · DZE Implant, Endosseous, Root-Form

Cleared on Nov 1, 2021 as substantially equivalent to K181138 (Neobiotech Co., Ltd., 2018) after a 252-day review. Its family tree reaches back 11 generations to 1990. 1 later device descends from it.

Decided
Nov 1, 2021
Review
252 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K894595 (1990). 27 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 7 generations between
  3. 3 generations backK090825 SQ IS SystemNeobiotech Co., Ltd. · 2009
  4. 2 generations backK113554 Cmi Implant IS SystemNeobiotech Co., Ltd. · 2012
  5. 1 generation backK181138 IS-III active SystemNeobiotech Co., Ltd. · 2018
  6. This deviceK210499 Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH · 2021
  7. Descendant · cites it directly · 0 of its ownK240435 Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH · 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 backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
  5. 7 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
  6. 6 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
  7. 5 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
  8. 4 generations backK073465 US/GS Ultra Wide SystemOsstem Implant Co., Ltd. · 2008
  9. 3 generations backK090825 SQ IS SystemNeobiotech Co., Ltd. · 2009
  10. 2 generations backK113554 Cmi Implant IS SystemNeobiotech Co., Ltd. · 2012
  11. 1 generation backK181138 IS-III active SystemNeobiotech Co., Ltd. · 2018
  12. This deviceK210499 Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH · 2021

Most influential descendants

Showing 1 of 1 · See all
  • K240435Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH · 2024 · cites it directly0descendants
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—
−8K0118793A Dental Implant SystemOsseco Biosource, Ltd.2002—
−7K051576Avana Dental Implant SystemOsstem Co., Ltd.2005—
−6K062051SS SystemOsstem Implant Co., Ltd.2006—
−5K063861GS SystemOsstem Implant Co., Ltd.2007—
−4K073465US/GS Ultra Wide SystemOsstem Implant Co., Ltd.2008—
−3K090825SQ IS SystemNeobiotech Co., Ltd.2009—
−2K113554Cmi Implant IS SystemNeobiotech Co., Ltd.2012—
−1K181138IS-III active SystemNeobiotech Co., Ltd.2018—
0 (this device)K210499Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH2021—
+1K240435Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199420
199620
199710
199810
200020
200110
200210
200510
200620
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K210499, 1990–2024Source: 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? (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
*K181138IS-III active System
Summary page 4
…NHA CFR section: 21 CFR872.3640 Device panel: Dental Legally Marketed Primary Predicate Device: K181138 - IS-III active System, Neobiotech Co., Ltd Legally Marketed Reference Devices: K180968 – Alpha Dent I…
Neobiotech Co., Ltd.2018—
†K180968AlphaDent Implants Dental Implants SystemAlphadent Implants, Ltd.2019—
†K181381A.B. Dental Devices Dental Implants SystemA.B. Dental Device, Ltd.2018—

Also cleared against K181138: 10 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
K240435Alpha Dent Implants Dental Implants SystemAlpha Dent Implants GmbH20240

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 31 years and passes through 8 companies; a new generation was cleared every 2.6 years on median.
  • 1 of the 27 ancestors has a recall of any class.
  • Of its descendants, K240435 (Alpha Dent Implants GmbH, 2024) has gone furthest, with 0 descendants of its own.
  • 10 other devices also cite its predicate K181138.

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. 2021, 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?

Alpha Dent Implants Dental Implants System is intended for surgical placement in the maxillary and/or the mandibular arch, to support crowns, bridges, or over dentures, in edentulous patients. It is intended to provide support for prosthetic devices, such as artificial teeth, and to restore the patient's chewing function. The System is intended to be used in either single tooth or multiple teeth applications. The prostheses can be screw or cement retained to the abutment.

The Alpha Dent Implants Dental Implants System is indicated also, for immediate loading when good primary stability is achieved and with appropriate occlusal loading.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K210499: Alpha Dent Implants Dental Implants System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210499

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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