510(k) Report

FDA product code · Dental

Resin, Root Canal Filling Containing Chloroform

MMTClass III21 CFR 872.3820PMA required0 decisions0 recalls

0 FDA decisions. No recall names this code.

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

FIG. A — Illustration, dental panel

Twenty years of MMT at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · MMT

FDA has decided no MMT device since 2007.

Median 510(k) review, days · MMT

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

Recalls per year · MMT

No recall names MMT since 2007.

Adverse event reports per year · MMT

1in 2022

2021: 12022: 1
2007high 1 (2021) · low 0 (2007)2025

MAUDE reports naming product code MMT, 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—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—01
20220—01
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — MMT by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MMT? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 872.3820.

KIF Resin, Root Canal FillingNYD Endodontic Kit