510(k) Report

De Novo · Granted

Granted

Eclipse System

DEN140020De NovoGranted Feb 12, 2015233-day reviewClass II21 CFR 876.5930

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

Pelvalon · PJH Dynamic Rectal Control System

Granted on Feb 12, 2015 as a new device type through De Novo after a 233-day review. 1 later device descends from it.

Decided
Feb 12, 2015
Review
233 days
Class
Class II
Product code
PJH
Recalls
None

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2015: 1 descendant cleared201620182020202220242026
  1. This deviceDEN140020 Eclipse SystemPelvalon · 2015
  2. Descendant · cites it directly · 0 of its ownK150558 Eclipse SystemPelvalon, Inc. · 2015

Most influential descendants

Showing 1 of 1 · See all
  • K150558Eclipse SystemPelvalon, Inc. · 2015 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)DEN140020Eclipse SystemPelvalon2015—
+1K150558Eclipse SystemPelvalon, Inc.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
FIG. 1 — Lineage of DEN140020, 2015–2015Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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

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

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

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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Does it have a predicate?

De Novo decisions do not claim a predicate device.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K150558Eclipse SystemPelvalon, Inc.20150

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.

What does this lineage say?

  • Of its descendants, K150558 (Pelvalon, Inc., 2015) has gone furthest, with 0 descendants of its own.

How does its category compare?

All PJH devices

PJH Dynamic Rectal Control System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · PJH

2in 2015

2015: 2
2007high 2 (2015) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PJH

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

Recalls per year · PJH

No recall names PJH since 2007.

Adverse event reports per year · PJH

No MAUDE report names PJH since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20152—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

The Eclipse System, a prescription device under 21 CFR Part 801.109 that is indicated for the treatment of fecal incontinence in adult women.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “DEN140020: Eclipse System.” Lineage record from FDA De Novo data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/DEN140020

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026