510(k) Report

510(k) · Cleared

Cleared

Enamel Microabrasion Compound

K891536510(k) TraditionalCleared Jun 9, 198984-day reviewClass I21 CFR 872.6030

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

Premier Dental Products Co. · EJR Agent, Polishing, Abrasive, Oral Cavity

Cleared on Jun 9, 1989 after an 84-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jun 9, 1989
Review
84 days
Class
Class I
Product code
EJR
Recalls
None
Predicates
0

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

Descendants, by year cleared 2008: 1 descendant cleared1990200020102020
  1. This deviceK891536 Enamel Microabrasion CompoundPremier Dental Products Co. · 1989
  2. Descendant · cites it directly · 0 of its ownK081493 Infiltration KitDmg USA, Inc. · 2008

Most influential descendants

Showing 1 of 1 · See all
  • K081493Infiltration KitDmg USA, Inc. · 2008 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K891536Enamel Microabrasion CompoundPremier Dental Products Co.1989—
+1K081493Infiltration KitDmg USA, Inc.2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
FIG. 1 — Lineage of K891536, 1989–2008Source: 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 EJR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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? (1)

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

NumberDeviceApplicantDecidedDescendants
K081493Infiltration KitDmg USA, Inc.20080

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, K081493 (Dmg USA, Inc., 2008) has gone furthest, with 0 descendants of its own.

How does its category compare?

All EJR devices

EJR Agent, Polishing, Abrasive, Oral Cavity: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EJR

1in 2017

2007: 12010: 22011: 22012: 12014: 12017: 1
2007high 2 (2010) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EJR

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

Recalls per year · EJR

No recall names EJR since 2007.

Adverse event reports per year · EJR

4in 2025

2007: 62009: 22010: 32011: 12012: 32013: 92014: 22015: 102016: 92017: 32019: 82020: 32021: 62022: 22023: 32025: 4
2007high 10 (2015) · low 0 (2008)2025

MAUDE reports naming product code EJR, 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—06
20080—00
20090—02
20102—03
20112—01
20121—03
20130—09
20141—02
20150—010
20160—09
20171—03
20180—00
20190—08
20200—03
20210—06
20220—02
20230—03
20240—00
20250—04
20260—0—
Cite this page

510(k) Report. “K891536: Enamel Microabrasion Compound.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K891536

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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