510(k) Report

FDA product code · General and plastic surgery

Laser, Cellulite Appearance

OYWClass II21 CFR 878.4810510(k) required2 decisions since 20120 recalls

2 FDA decisions since 2012. No recall names this code. The most-cited predicate is K102541, named by 2 later devices.

For the removal of fat through laser lipolysis.

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 OYW 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 · OYW

1in 2013

2012: 12013: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OYW

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

Recalls per year · OYW

No recall names OYW since 2007.

Adverse event reports per year · OYW

2in 2019

2013: 12015: 32016: 22019: 2
2007high 3 (2015) · low 0 (2007)2025

MAUDE reports naming product code OYW, 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
20121—00
20131—01
20140—00
20150—03
20160—02
20170—00
20180—00
20190—02
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — OYW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OYW? 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 878.4810.