510(k) · Cleared

Cleared

Aigis-Fine

K024143510(k) TraditionalCleared Mar 10, 200384-day reviewClass II21 CFR 872.3060

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

Sb Lucius, Inc. · EJT Alloy, Gold-Based Noble Metal

Cleared on Mar 10, 2003 as substantially equivalent to K993475 (Metalor Dental USA Corp., 1999) after an 84-day review. Its family tree reaches back 1 generation to 1999.

Decided: Mar 10, 2003
Review: 84 days
Class: Class II
Product code: EJT
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K993475 (1999). No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK993475 Aurofluid M, Alloy NO. 5315Metalor Dental USA Corp. · 1999
This deviceK024143 Aigis-FineSb Lucius, Inc. · 2003

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K993475	Aurofluid M, Alloy NO. 5315	Metalor Dental USA Corp.	1999	—
0 (this device)	K024143	Aigis-Fine	Sb Lucius, Inc.	2003	—

FIG. 1 — Lineage of K024143, 1999–2003Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 EJT? 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? (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.

Type	Number	Device	Applicant	Decided	Recalls
*	K993475	Aurofluid M, Alloy NO. 5315 Summary page 1 …EJT Classification : Class II Legally marketed device: AUROFLUID M 51 O(k) number: K993475 SUMMARY OF THE TECHNOLOGICAL CHARACTERISTICS Test methods applied: as in ANSVADA 5 and I…	Metalor Dental USA Corp.	1999	—

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.

What does this lineage say?

Its one ancestor has no recall.

How does its category compare?

All EJT devices

EJT Alloy, Gold-Based Noble Metal: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EJT

FDA has decided no EJT device since 2007.

Median 510(k) review, days · EJT

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

Recalls per year · EJT

No recall names EJT since 2007.

Adverse event reports per year · EJT

1in 2017

2007high 1 (2011) · low 0 (2007)2025

MAUDE reports naming product code EJT, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	1
2012	—	0
2013	—	0
2014	—	1
2015	—	0
2016	—	1
2017	—	1
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

What is it indicated for?

AIGIS-FINE is intended for manufacturing

- Inlay / Onlays

- Crowns

- Short span bridges

- Long span bridges

- Removable partials

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K024143 · printed Nov 3, 2026

Cite this page

510(k) Report. “K024143: Aigis-Fine.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K024143

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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