510(k) Report

FDA product code · Gastroenterology and urology

Mini Endoscope, Gastroenterology-Urology

ODFClass II21 CFR 876.1500510(k) required12 decisions since 19880 recalls

12 FDA decisions since 1988. No recall names this code. The most-cited predicate is K050403, named by 4 later devices.

To examine and perform procedures in body cavities of the GI and GU tract. If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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 ODF 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 · ODF

1in 2010

2009: 22010: 1
2007high 2 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ODF

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

Recalls per year · ODF

No recall names ODF since 2007.

Adverse event reports per year · ODF

1in 2022

2008: 52009: 42010: 12011: 52012: 42013: 32014: 22015: 12016: 12017: 12022: 1
2007high 5 (2008) · low 0 (2007)2025

MAUDE reports naming product code ODF, 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—05
20092—04
20101—01
20110—05
20120—04
20130—03
20140—02
20150—01
20160—01
20170—01
20180—00
20190—00
20200—00
20210—00
20220—01
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — ODF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ODF? 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 876.1500.