510(k) Report

FDA product code · Dental

Stimulator, Muscle, Powered, Dental

NUWClass II21 CFR 890.5850510(k) required9 decisions since 19770 recalls

9 FDA decisions since 1977. 510(k) reviews decided 2021–2025 took a median of 179 days (half between 167 and 191). No recall names this code. The most-cited predicate is K031998, named by 4 later devices.

Relief of muscle spasms associated with tmj. Muscle reeducation, increasing blood flow.

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 NUW 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 · NUW

1in 2025

2021: 12025: 1
2007high 1 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NUW

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

Recalls per year · NUW

No recall names NUW since 2007.

Adverse event reports per year · NUW

No MAUDE report names NUW since 2007.

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
20211—00
20220—00
20230—00
20240—00
20251—00
20260—0—
FIG. 1 — NUW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NUW? 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 890.5850.