510(k) Report

FDA product code · General and plastic surgery

Laser Assisted Lipolysis

ORKClass II21 CFR 878.4810510(k) required1 decision since 20110 recalls

1 FDA decision since 2011. No recall names this code.

Intended to be used for laser assisted 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 ORK 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 · ORK

1in 2011

2011: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ORK

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

Recalls per year · ORK

No recall names ORK since 2007.

Adverse event reports per year · ORK

1in 2024

2018: 22024: 1
2007high 2 (2018) · low 0 (2007)2025

MAUDE reports naming product code ORK, 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
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—02
20190—00
20200—00
20210—00
20220—00
20230—00
20240—01
20250—00
20260—0—
FIG. 1 — ORK by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ORK? 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.