510(k) Report

FDA product code · General and plastic surgery

Instrument For Treatment Of Hyperhidrosis

OUBClass II21 CFR 878.4400510(k) required3 decisions since 20112 recalls

3 FDA decisions since 2011. 2 recalls name this code, 0 of them Class I. The most-cited predicate is K103014, named by 2 later devices.

Soft-tissue coagulation

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 OUB 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 · OUB

1in 2015

2011: 12013: 12015: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OUB

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

Recalls per year · OUB

1in 2015

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

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

Adverse event reports per year · OUB

52in 2025

2013: 82014: 142015: 582016: 652017: 482018: 1312019: 962020: 392021: 122022: 412023: 492024: 202025: 52
2007high 131 (2018) · low 0 (2007)2025

MAUDE reports naming product code OUB, 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—10
20120—00
20131—08
20140—014
20151—158
20160—065
20170—048
20180—0131
20190—096
20200—039
20210—012
20220—041
20230—049
20240—020
20250—052
20260—0—
FIG. 1 — OUB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OUB? 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.