510(k) Report

510(k) · Cleared

Cleared

Zest Implant Anchor Advanced Generation (Dental)

K934668510(k) TraditionalCleared Jun 22, 1994266-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

Zest Anchors, Inc. · DZE Implant, Endosseous, Root-Form

Cleared on Jun 22, 1994 after a 266-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 186 later devices descend from it.

Decided
Jun 22, 1994
Review
266 days
Class
Class II
Product code
DZE
Recalls
None
Predicates
0

186 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2000: 1 descendant cleared2014: 11 descendants cleared2012: 4 descendants cleared2009: 2 descendants cleared2007: 1 descendant cleared2011: 2 descendants cleared2013: 3 descendants cleared2010: 1 descendant cleared2018: 8 descendants cleared2025: 25 descendants cleared2015: 7 descendants cleared2020: 13 descendants cleared2021: 14 descendants cleared2022: 18 descendants cleared2019: 12 descendants cleared2016: 7 descendants cleared2017: 3 descendants cleared2024: 20 descendants cleared2023: 19 descendants cleared2026: 15 descendants cleared1990200020102020
  1. This deviceK934668 Zest Implant Anchor Advanced Generation (Dental)Zest Anchors, Inc. · 1994
  2. Descendant · cites it directly · 185 of its ownK994257 Locator Implant AnchorZest Anchors, Inc. · 2000 · Recalled
  3. Descendant · 2 generations on · 134 of its ownK092594 Ace Surgical Secure- Mini Locator Implant System, Model 09-2702-OX…Ace Surgical Supply Co., Inc. · 2009
  4. Descendant · 3 generations on · 127 of its ownK123022 Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2013
  5. Descendant · 4 generations on · 123 of its ownK133510 Neodent Implant SystemJj Industria E Comercio DE Materiais Dentarios SA · 2014
  6. Descendant · 4 generations on · 109 of its ownK133592 Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua…Neodent USA, Inc. · 2014

Showing 5 of 186 descendants. See all descendants

Descendants cleared per year

2000: 12007: 12009: 22010: 12011: 22012: 42013: 32014: 112015: 72016: 72017: 32018: 82019: 122020: 132021: 142022: 182023: 192024: 202025: 252026: 15
2000high 25 (2025) · low 0 (2001)2026

Most influential descendants

Showing 5 of 186 · See all
  • K994257Locator Implant AnchorZest Anchors, Inc. · 2000 · cites it directly185descendants
  • K092594Ace Surgical Secure- Mini Locator Implant System, Model 09-2702-OX, 09-2703-OX, 09-2705-OXAce Surgical Supply Co., Inc. · 2009 · 2 generations on134descendants
  • K123022Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S · 2013 · 3 generations on127descendants
  • K133510Neodent Implant SystemJj Industria E Comercio DE Materiais Dentarios SA · 2014 · 4 generations on123descendants
  • K133592Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua, Titamax Smart EX Acqua…Neodent USA, Inc. · 2014 · 4 generations on109descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K934668Zest Implant Anchor Advanced Generation (Dental)Zest Anchors, Inc.1994—
+1K994257Locator Implant AnchorZest Anchors, Inc.20002
+2K092594Ace Surgical Secure- Mini Locator Implant System, Model 09-2702-OX…Ace Surgical Supply Co., Inc.2009—
+3K123022Neodent Implant SystemJjgc Industria E Comercio DE Materiais Dentarios S2013—
+4K133510Neodent Implant SystemJj Industria E Comercio DE Materiais Dentarios SA2014—
+4K133592Neodent Implant System, Titamax TI EX Acqua and TI Drive Acqua, Titamax Smart…Neodent USA, Inc.2014—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200010
200710
200920
201010
201120
201240
201330
2014110
201570
201670
201730
201880
2019120
2020130
2021140
2022180
2023190
2024200
2025250
2026150
FIG. 1 — Lineage of K934668, 1994–2026Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (186)

See all 186

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K994257Locator Implant AnchorZest Anchors, Inc.2000185

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?

  • Of its descendants, K994257 (Zest Anchors, Inc., 2000) has gone furthest, with 185 descendants of its own.

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—

More from Zest Anchors, Inc.

14 FDA decisions under this applicant name. See the company

  • K150295LOCATOR RTxZest Anchors, Inc. · 2015
  • K083324Locator Implant Anchor Attachment SystemZest Anchors, Inc. · 2009
  • K072878Modification to: Locator Implant AnchorZest Anchors, Inc. · 20071 recall
  • K042466X-2 Implant Abutment; Bar Male; Distal Extension MaleZest Anchors, Inc. · 2004
  • K033699Locator Bar Female, Locator Laser Bar Female, Locator Bar Cast-to Female, Models 08587, 08588, 08586Zest Anchors, Inc. · 2004

Recent decisions in DZE

The DZE category page

  • K261295MultiNeO Dental Implant SystemAlpha Bio Tec, Ltd. · 2026
  • K261392TriActive Dental Implant SystemParagon Implant Mfg., LLC · 2026
  • K260463ZEROS Dental Implant SystemZeros Co., Ltd. · 2026
  • K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd. · 2026
  • K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd. · 2026

https://510kreport.com/device/K934668 · printed Nov 6, 2026

Cite this page

510(k) Report. “K934668: Zest Implant Anchor Advanced Generation (Dental).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K934668

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026