510(k) Report

510(k) · Cleared

Cleared

A-Company Elastomeric Tubing

K852599510(k) TraditionalCleared Jul 31, 198542-day reviewClass I21 CFR 872.5410

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

A Company, Inc. · ECI Band, Elastic, Orthodontic

Cleared on Jul 31, 1985 after a 42-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Jul 31, 1985
Review
42 days
Class
Class I
Product code
ECI
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K852599Source: FDA 510(k) database · 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.

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  • 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?

No later submission names this one as a predicate yet.

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.

How does its category compare?

All ECI devices

ECI Band, Elastic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · ECI

FDA has decided no ECI device since 2007.

Median 510(k) review, days · ECI

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

Recalls per year · ECI

1in 2023

2011: 12023: 1
2007high 1 (2011) · low 0 (2007)2026

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

Adverse event reports per year · ECI

1in 2024

2007: 12012: 12014: 22015: 12016: 12017: 12018: 12020: 22023: 42024: 1
2007high 4 (2023) · low 0 (2008)2025

MAUDE reports naming product code ECI, 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—01
20080—00
20090—00
20100—00
20110—10
20120—01
20130—00
20140—02
20150—01
20160—01
20170—01
20180—01
20190—00
20200—02
20210—00
20220—00
20230—14
20240—01
20250—00
20260—0—
Cite this page

510(k) Report. “K852599: A-Company Elastomeric Tubing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K852599

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026