510(k) Report

FDA product code · Dental

Prosthesis, Condyle, Mandibular, Temporary

NEIClass II21 CFR 872.4770510(k) required7 decisions since 19990 recalls

7 FDA decisions since 1999. No recall names this code. The most-cited predicate is K990667, named by 3 later devices.

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 NEI 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 · NEI

1in 2014

2007: 12008: 12014: 1
2007high 1 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NEI

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

Recalls per year · NEI

No recall names NEI since 2007.

Adverse event reports per year · NEI

2in 2024

2013: 12014: 32015: 12018: 32019: 62021: 82024: 2
2007high 8 (2021) · low 0 (2007)2025

MAUDE reports naming product code NEI, 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—00
20081—00
20090—00
20100—00
20110—00
20120—00
20130—01
20141—03
20150—01
20160—00
20170—00
20180—03
20190—06
20200—00
20210—08
20220—00
20230—00
20240—02
20250—00
20260—0—
FIG. 1 — NEI by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NEI? 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