510(k) Report

510(k) · Cleared

Cleared

Microetcher

K902836510(k) TraditionalCleared Nov 20, 1990145-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 Nov 20, 1990 after a 145-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Nov 20, 1990
Review
145 days
Class
Class II
Product code
KOJ
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1996: 1 descendant cleared1990200020102020
  1. This deviceK902836 MicroetcherDanville Engineering, Inc. · 1990
  2. Descendant · cites it directly · 0 of its ownK984415 S.S. White Technologies, Models 6500-D,6500-E, and 6500-FS.S. White Technologies, Inc. · 1999
  3. Descendant · cites it directly · 0 of its ownK963735 Cojet SystemEspe GmbH & Co. Kg. · 1996

Most influential descendants

Showing 2 of 2 · See all
  • K984415S.S. White Technologies, Models 6500-D,6500-E, and 6500-FS.S. White Technologies, Inc. · 1999 · cites it directly0descendants
  • K963735Cojet SystemEspe GmbH & Co. Kg. · 1996 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K902836MicroetcherDanville Engineering, Inc.1990—
+1K984415S.S. White Technologies, Models 6500-D,6500-E, and 6500-FS.S. White Technologies, Inc.1999—
+1K963735Cojet SystemEspe GmbH & Co. Kg.1996—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199910
FIG. 1 — Lineage of K902836, 1990–1999Source: 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), 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
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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? (2)

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

NumberDeviceApplicantDecidedDescendants
K984415S.S. White Technologies, Models 6500-D,6500-E, and 6500-FS.S. White Technologies, Inc.19990
K963735Cojet SystemEspe GmbH & Co. Kg.19960

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, K984415 (S.S. White Technologies, Inc., 1999) 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—
Cite this page

510(k) Report. “K902836: Microetcher.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K902836

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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