510(k) Report

FDA product code · General and plastic surgery

Dermal Cooling Pack/Vacuum/Massager

OOKClass II21 CFR 878.4340510(k) required14 decisions since 20100 recalls

14 FDA decisions since 2010. 510(k) reviews decided 2021–2025 took a median of 184 days (half between 127 and 240). No recall names this code. The most-cited predicate is DEN090002, named by 4 later devices.

The device is a combination of a cooling pad associated with a vacuum or mechanical massager intended for the disruption or induction of adipocyte cells indicated for body contouring or reduction in circumference of body areas.

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 OOK 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 · OOK

1in 2024

2010: 12012: 12014: 12015: 22016: 22017: 22018: 12019: 12020: 12021: 12024: 1
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OOK

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

Recalls per year · OOK

No recall names OOK since 2007.

Adverse event reports per year · OOK

901in 2025

2011: 52012: 322013: 292014: 52015: 82016: 212017: 92018: 102019: 492020: 182021: 1,1612022: 1,9782023: 5,4992024: 1,2772025: 901
2007high 5,499 (2023) · low 0 (2007)2025

MAUDE reports naming product code OOK, 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
20101—00
20110—05
20121—032
20130—029
20141—05
20152—08
20162—021
20172—09
20181—010
20191—049
20201—018
20211—01,161
20220—01,978
20230—05,499
20241—01,277
20250—0901
20260—0—
FIG. 1 — OOK by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OOK? 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 878.4340.