510(k) Report

510(k) · Cleared

Recalled · Class II · 2020

Neocis Guidance System (NGS) with Chairside Splint

K173402510(k) TraditionalCleared Feb 22, 2018114-day reviewClass II21 CFR 872.4120Recalls 4

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

Neocis, Inc. · PLV Dental Stereotaxic Instrument

Cleared on Feb 22, 2018 as substantially equivalent to K161399 (Neocis, Inc., 2016) after a 114-day review. Its family tree reaches back 4 generations to 1999. 5 later devices descend from it. It has been recalled 4 times.

Decided
Feb 22, 2018
Review
114 days
Class
Class II
Product code
PLV
Recalls
4
Predicates
1

Its longest line of descent runs back 4 generations to K983831 (1999). 5 ancestors in all. 5 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 1 other ancestor2020: 2 descendants cleared2018: 1 descendant cleared2019: 2 descendants clearedK983831 · VECTORVISION2 · Brainlab AG · 1999K023424 · Igi-System · Denx Advanced Dental Systems · 2003K150222 · X-Guide Surgical Navigation System · X-Nav Technologies, LLC · 2015 · recalledK161399 · Neocis Guidance System · Neocis, Inc. · 2016 · recalled1995200020052010201520202025
Other ancestors, by generationDescendants, by generation 4 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 2 descendants K161399 · Neocis Guidance System · Neocis, Inc. · 2016 · recalledK150222 · X-Guide Surgical Navigation System · X-Nav Technologies, LLC · 2015 · recalledK023424 · Igi-System · Denx Advanced Dental Systems · 2003K983831 · VECTORVISION2 · Brainlab AG · 19990
  1. Root · 4 generations backK983831 VECTORVISION2Brainlab AG · 1999
  2. 3 generations backK023424 Igi-SystemDenx Advanced Dental Systems · 2003
  3. 2 generations backK150222 X-Guide Surgical Navigation SystemX-Nav Technologies, LLC · 2015 · Recalled
  4. 1 generation backK161399 Neocis Guidance SystemNeocis, Inc. · 2016 · Recalled
  5. This deviceK173402 Neocis Guidance System (NGS) with Chairside SplintNeocis, Inc. · 2018
  6. Descendant · cites it directly · 2 of its ownK182776 Neocis Guidance SystemNeocis, Inc. · 2018
  7. Descendant · cites it directly · 0 of its ownK202100 Neocis Guidance System (NGS) with Clamped Chairside Patient Splint…Neocis, Inc. · 2020
  8. Descendant · cites it directly · 0 of its ownK200348 Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)Neocis, Inc. · 2020
  9. Descendant · 2 generations on · 0 of its ownK191363 Neocis Planning Software Application (NPSA) for 3rd Party PCsNeocis, Inc. · 2019
  10. Descendant · 2 generations on · 0 of its ownK191605 Neocis Guidance System (NGS)Neocis, Inc. · 2019

Most influential descendants

Showing 5 of 5 · See all
  • K182776Neocis Guidance SystemNeocis, Inc. · 2018 · cites it directly2descendants
  • K202100Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)Neocis, Inc. · 2020 · cites it directly0descendants
  • K200348Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)Neocis, Inc. · 2020 · cites it directly0descendants
  • K191363Neocis Planning Software Application (NPSA) for 3rd Party PCsNeocis, Inc. · 2019 · 2 generations on0descendants
  • K191605Neocis Guidance System (NGS)Neocis, Inc. · 2019 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K983831VECTORVISION2Brainlab AG1999—
−3K023424Igi-SystemDenx Advanced Dental Systems2003—
−2K150222X-Guide Surgical Navigation SystemX-Nav Technologies, LLC20151
−1K161399Neocis Guidance SystemNeocis, Inc.20161
0 (this device)K173402Neocis Guidance System (NGS) with Chairside SplintNeocis, Inc.2018—
+1K182776Neocis Guidance SystemNeocis, Inc.2018—
+1K202100Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)Neocis, Inc.2020—
+1K200348Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)Neocis, Inc.2020—
+2K191363Neocis Planning Software Application (NPSA) for 3rd Party PCsNeocis, Inc.2019—
+2K191605Neocis Guidance System (NGS)Neocis, Inc.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
201920
202020
FIG. 1 — Lineage of K173402, 1999–2020Source: 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 PLV? 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 PLV device

  1. #1 K231018 Yomi Robotic Systemscore 13.9 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K161399Neocis Guidance System
Summary page 4
…one cutting instrument and accessories (21 CFR 872.4120) Classification: Class II Product Code: PLV Predicate Device: Neocis Guidance System (K161399) Indications for Use: The Neocis Guidance System (NGS) is a computerized navigational system intended to provide assistance in b…
Neocis, Inc.20161

Also cleared against K161399: 2 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K182776Neocis Guidance SystemNeocis, Inc.20182
K202100Neocis Guidance System (NGS) with Clamped Chairside Patient Splint (C-CPS)Neocis, Inc.20200
K200348Neocis Guidance System (NGS) with Fiducial Array Splint (FAS)Neocis, Inc.20200

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Oct 30, 2020Class IIZ-0929-2021Process controlThe LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.
May 14, 2020Class IIZ-2639-2020Process controlThe LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
May 14, 2020Class IIZ-2638-2020Process controlThe LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
May 14, 2020Class IIZ-2637-2020Process controlThe LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 19 years and passes through 4 companies; a new generation was cleared every 4.0 years on median.
  • 2 of the 5 ancestors have a recall of any class.
  • Of its descendants, K182776 (Neocis, Inc., 2018) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K161399.

How does its category compare?

All PLV devices

PLV Dental Stereotaxic Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · PLV

2in 2025

2015: 12016: 22018: 22019: 22020: 72021: 22022: 32023: 12024: 12025: 2
2007high 7 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PLV

399in 2022

2020: 86 days median2022: 399 days median
2007high 399 (2022) · low 86 (2020)2026

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

Recalls per year · PLV

1in 2020

2019: 12020: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · PLV

6in 2025

2019: 32021: 112022: 392023: 152024: 92025: 6
2007high 39 (2022) · low 0 (2007)2025

MAUDE reports naming product code PLV, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20151—00
20162—00
20170—00
20182—00
20192—13
202078610
20212—011
20223399039
20231—015
20241—09
20252—06
20260—0—

What is it indicated for?

The Neocis Guidance System (NGS) is a computerized navigational system intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery. The system provides software to preoperatively plan dental implantation procedures and provides navigational guidance of the surgical instruments.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K173402: Neocis Guidance System (NGS) with Chairside Splint.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K173402

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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