FDA product code · Dental

Injector, Jet, Gas-Powered

Name: FDA decisions, review times, recalls and adverse event reports for product code EGQ
Creator: 510(k) Report

EGQClass II21 CFR 872.4465510(k) required1 decision since 19900 recalls

1 FDA decision since 1990. 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 EGQ 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 · EGQ

FDA has decided no EGQ device since 2007.

Median 510(k) review, days · EGQ

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

Recalls per year · EGQ

No recall names EGQ since 2007.

Adverse event reports per year · EGQ

No MAUDE report names EGQ since 2007.

View these four charts as a table

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

FIG. 1 — EGQ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in EGQ? 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

Injector, Jet, Gas-Powered

What has FDA decided in EGQ lately?