510(k) Report

FDA product code · Physical medicine

Adhesive Backed Thermal Skin Patches

OMWClass I21 CFR 890.5710510(k) exempt0 decisions0 recalls

FDA lists OMW as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 890.9 applies, such as a new intended use or a different fundamental technology. 0 FDA decisions. No recall names this code.

Pain relief heat patches for temporary relief of muscular and joint pian assoiciated with arthritis, simple backache, muscle strains and sprains.External use only. Not on damaged skin or open sores. Do no use under the age of 12. Do use on people who are not able to feel pain. Patch is applied directly to site of pain over intact skin for up to 8 hours but not more than once in a 24 hour period. Do not use more…

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, physical medicine panel

Twenty years of OMW 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 · OMW

FDA has decided no OMW device since 2007.

Median 510(k) review, days · OMW

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

Recalls per year · OMW

No recall names OMW since 2007.

Adverse event reports per year · OMW

5in 2025

2008: 32009: 162010: 52011: 32012: 42016: 12019: 12023: 22024: 22025: 5
2007high 16 (2009) · low 0 (2007)2025

MAUDE reports naming product code OMW, 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—03
20090—016
20100—05
20110—03
20120—04
20130—00
20140—00
20150—00
20160—01
20170—00
20180—00
20190—01
20200—00
20210—00
20220—00
20230—02
20240—02
20250—05
20260—0—
FIG. 1 — OMW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OMW? 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 890.5710.