510(k) Report

510(k) · Cleared

Cleared

Gentle Colonics Irrigation System

K002102510(k) TraditionalCleared Feb 6, 2002574-day reviewClass II21 CFR 876.5220

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Gentle Colonics, Inc. · KPL Colonic Irrigation System

Cleared on Feb 6, 2002 after a 574-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Feb 6, 2002
Review
574 days
Class
Class II
Product code
KPL
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K002102Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KPL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new KPL device

  1. #1 K201861 Bio Fluff Systemscore 3.5 · 3 generations · no Class I recall
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All KPL devices

KPL Colonic Irrigation System: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KPL

1in 2022

2007: 12010: 12014: 12015: 12016: 12018: 12022: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPL

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

Recalls per year · KPL

No recall names KPL since 2007.

Adverse event reports per year · KPL

1in 2017

2007: 22010: 22013: 12017: 1
2007high 2 (2007) · low 0 (2008)2025

MAUDE reports naming product code KPL, 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
20071—02
20080—00
20090—00
20101—02
20110—00
20120—00
20130—01
20141—00
20151—00
20161—00
20170—01
20181—00
20190—00
20200—00
20210—00
20221—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K002102: Gentle Colonics Irrigation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K002102

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026