510(k) Report

FDA product code · Gastroenterology and urology

Collector, Ostomy

EXBClass I21 CFR 876.5900510(k) exempt102 decisions since 19765 recalls

FDA lists EXB as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 876.9 applies, such as a new intended use or a different fundamental technology. 102 FDA decisions since 1976. 510(k) reviews decided 2021–2025 took a median of 90 days (half between 90 and 90). 5 recalls name this code, 0 of them Class I. The most-cited predicate is K140938, named by 2 later devices.

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, gastroenterology and urology panel

Twenty years of EXB 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 · EXB

1in 2025

2014: 12018: 12025: 1
2007high 1 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EXB

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

Recalls per year · EXB

3in 2011

2008: 22011: 3
2007high 3 (2011) · low 0 (2007)2026

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

Adverse event reports per year · EXB

20in 2025

2008: 12009: 12010: 52011: 42012: 72013: 1872014: 552015: 62016: 202017: 202018: 362019: 342020: 222021: 422022: 362023: 112024: 132025: 20
2007high 187 (2013) · low 0 (2007)2025

MAUDE reports naming product code EXB, 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—21
20090—01
20100—05
20110—34
20120—07
20130—0187
20141—055
20150—06
20160—020
20170—020
20181—036
20190—034
20200—022
20210—042
20220—036
20230—011
20240—013
20251—020
20260—0—
FIG. 1 — EXB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in EXB? 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 876.5900.