510(k) Report

510(k) · Cleared

Cleared

Microetcher AP

K970589510(k) TraditionalCleared Sep 17, 1997211-day reviewClass II21 CFR 872.6080

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

Danville Engineering, Inc. · KOJ Airbrush

Cleared on Sep 17, 1997 after a 211-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
Sep 17, 1997
Review
211 days
Class
Class II
Product code
KOJ
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared1995200020052010201520202025
  1. This deviceK970589 Microetcher APDanville Engineering, Inc. · 1997
  2. Descendant · cites it directly · 0 of its ownK033215 PrepairDanville Materials, Inc. · 2004

Most influential descendants

Showing 1 of 1 · See all
  • K033215PrepairDanville Materials, Inc. · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K970589Microetcher APDanville Engineering, Inc.1997—
+1K033215PrepairDanville Materials, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of K970589, 1997–2004Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KOJ? 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 KOJ device

  1. #1 K251425 turbodent touchscore 11.1 · 7 generations · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K033215PrepairDanville Materials, Inc.20040

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, K033215 (Danville Materials, Inc., 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KOJ devices

KOJ Airbrush: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KOJ

1in 2025

2007: 12025: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KOJ

Too few KOJ 510(k)s in any year since 2007 to give a median.

Recalls per year · KOJ

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · KOJ

2in 2025

2007: 12008: 22009: 32010: 32011: 22012: 12015: 22017: 12025: 2
2007high 3 (2009) · low 0 (2013)2025

MAUDE reports naming product code KOJ, 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
20071—01
20080—02
20090—03
20100—13
20110—02
20120—01
20130—00
20140—00
20150—02
20160—00
20170—01
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20251—02
20260—0—

What is it indicated for?

Cutting and preparation of tooth structure, both enamel and dentin for all classes of cavity preparations. Removal of composite resin restorations. Surface roughening of enamel,dentin, and metal dental structures prior to adhesive resin bonding.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K970589: Microetcher AP.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K970589

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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