510(k) Report

FDA product code · General and plastic surgery

Skin Resurfacing Rf Applicator

OUHClass II21 CFR 878.4400510(k) required5 decisions since 20111 recall

5 FDA decisions since 2011. 1 recall names this code; it is not Class I. The most-cited predicate is K101510, named by 5 later devices.

Skin resurfacing

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, general and plastic surgery panel

Twenty years of OUH 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 · OUH

1in 2016

2011: 12012: 12014: 12015: 12016: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OUH

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

Recalls per year · OUH

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OUH

3in 2025

2017: 12020: 22021: 12025: 3
2007high 3 (2025) · low 0 (2007)2025

MAUDE reports naming product code OUH, 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
20111—00
20121—00
20130—00
20141—00
20151—00
20161—00
20170—01
20180—00
20190—00
20200—12
20210—01
20220—00
20230—00
20240—00
20250—03
20260—0—
FIG. 1 — OUH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OUH? 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 878.4400.