510(k) Report

510(k) · Cleared

Cleared

Impla-NX (Model: ISE-270M)

K201192510(k) TraditionalCleared May 21, 2021382-day reviewClass I21 CFR 872.4200

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

Micro-Nx Co., Ltd. · EBW Controller, Foot, Handpiece And Cord

Cleared on May 21, 2021 as substantially equivalent to K173905 (Nakanishi, Inc., 2018) after a 382-day review. Its family tree reaches back 4 generations to 2001. 1 later device descends from it.

Decided
May 21, 2021
Review
382 days
Class
Class I
Product code
EBW
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K002469 (2001). 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK002469 Implantmed SI-95 115 (100-130 V) and SI-95 230 (220-240 V)W&H Dentalwerk Buermoos GmbH · 2001
  2. 3 generations backK052741 Implantmed SI-915 (115V Version); Implantmed SI-923 (230V Version)…W&H Dentalwerk Buermoos GmbH · 2006
  3. 2 generations backK161957 W&H Implantmed SI-1015 incl. AccessoriesW&H Dentalwerk Burmoos GmbH · 2016
  4. 1 generation backK173905 Surgic Pro, Surgic Pro+Nakanishi, Inc. · 2018
  5. This deviceK201192 Impla-NX (Model: ISE-270M)Micro-Nx Co., Ltd. · 2021
  6. Descendant · cites it directly · 0 of its ownK231562 ELEC ENGINE (Model: ISE-170L)Micro-Nx Co., Ltd. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K231562ELEC ENGINE (Model: ISE-170L)Micro-Nx Co., Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K002469Implantmed SI-95 115 (100-130 V) and SI-95 230 (220-240 V)W&H Dentalwerk Buermoos GmbH2001—
−3K052741Implantmed SI-915 (115V Version); Implantmed SI-923 (230V Version) Incl.…W&H Dentalwerk Buermoos GmbH2006—
−2K161957W&H Implantmed SI-1015 incl. AccessoriesW&H Dentalwerk Burmoos GmbH2016—
−1K173905Surgic Pro, Surgic Pro+Nakanishi, Inc.2018—
0 (this device)K201192Impla-NX (Model: ISE-270M)Micro-Nx Co., Ltd.2021—
+1K231562ELEC ENGINE (Model: ISE-170L)Micro-Nx Co., Ltd.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K201192, 2001–2025Source: 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 EBW? 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 EBW device

  1. #1 K251701 Star E900 Electric Systemscore 12.2 · 6 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
*K173905Surgic Pro, Surgic Pro+
Summary page 4
…ion Name - Dental handpiece and accessories  Classification – 21CFR 872.4200 (Product Code: EBW) 3. Predicate Device  Surgic Pro by NSK Nakanishi, Inc (K173905) 4. Description: As an engine to operate and control handpiece used for dental implant surgery, this device is co…
Nakanishi, Inc.2018—

Also cleared against K173905: 3 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
K231562ELEC ENGINE (Model: ISE-170L)Micro-Nx Co., Ltd.20250

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 20 years and passes through 4 companies; a new generation was cleared every 4.9 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K231562 (Micro-Nx Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K173905.

How does its category compare?

All EBW devices

EBW Controller, Foot, Handpiece And Cord: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · EBW

3in 2025

2009: 52010: 12011: 32012: 12013: 12014: 32015: 12016: 12017: 42018: 12019: 22020: 12021: 22022: 62024: 42025: 32026 (partial year): 3
2007high 6 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBW

220in 2025

2009: 112 days median2011: 226 days median2014: 189 days median2017: 227 days median2022: 479 days median2024: 268 days median2025: 220 days median2026 (partial year): 269 days median
2007high 479 (2022) · low 112 (2009)2026

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

Recalls per year · EBW

1in 2013

2013: 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · EBW

13in 2025

2009: 162010: 182011: 12012: 52013: 12014: 42015: 132016: 62017: 132018: 462019: 552020: 712021: 572022: 312023: 172024: 142025: 13
2007high 71 (2020) · low 0 (2007)2025

MAUDE reports naming product code EBW, 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
20095112016
20101—018
2011322601
20121—05
20131—11
2014318904
20151—013
20161—06
20174227013
20181—046
20192—055
20201—071
20212—057
20226479031
20230—017
20244268014
20253220013
202632690—

What is it indicated for?

The Impla-NX (Model: ISE-270M) is intended for use in dental oral surgery and dental implant. The main unit is designed to be used with a specific dental micromotor that drives dental handpieces fitted with appropriate tools to cut hard tissues in the mouth.

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. “K201192: Impla-NX (Model: ISE-270M).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201192

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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