510(k) Report

510(k) · Cleared

Cleared

Oleeva Foam

K002109510(k) TraditionalCleared Aug 31, 200050-day reviewClass I21 CFR 878.4025

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

Bio Med Sciences, Inc. · MDA Elastomer, Silicone, For Scar Management

Cleared on Aug 31, 2000 after a 50-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Aug 31, 2000
Review
50 days
Class
Class I
Product code
MDA
Recalls
None
Predicates
0

2 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2002: 1 descendant cleared2003: 1 descendant cleared200020052010201520202025
  1. This deviceK002109 Oleeva FoamBio Med Sciences, Inc. · 2000
  2. Descendant · cites it directly · 1 of its ownK023136 Oleeva FabricBio Med Sciences, Inc. · 2002
  3. Descendant · 2 generations on · 0 of its ownK024160 Neosporin Scar SolutionWarner-Lambert Co. · 2003

Most influential descendants

Showing 2 of 2 · See all
  • K023136Oleeva FabricBio Med Sciences, Inc. · 2002 · cites it directly1descendant
  • K024160Neosporin Scar SolutionWarner-Lambert Co. · 2003 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K002109Oleeva FoamBio Med Sciences, Inc.2000—
+1K023136Oleeva FabricBio Med Sciences, Inc.2002—
+2K024160Neosporin Scar SolutionWarner-Lambert Co.2003—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200310
FIG. 1 — Lineage of K002109, 2000–2003Source: 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 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K023136Oleeva FabricBio Med Sciences, Inc.20021

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, K023136 (Bio Med Sciences, Inc., 2002) has gone furthest, with 1 descendant of its own.

How does its category compare?

All MDA devices

MDA Elastomer, Silicone, For Scar Management: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MDA

2in 2011

2009: 12011: 2
2007high 2 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MDA

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

Recalls per year · MDA

No recall names MDA since 2007.

Adverse event reports per year · MDA

3in 2025

2007: 32013: 22014: 12015: 22016: 52017: 32018: 22019: 52020: 42021: 32023: 82025: 3
2007high 8 (2023) · low 0 (2008)2025

MAUDE reports naming product code MDA, 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—03
20080—00
20091—00
20100—00
20112—00
20120—00
20130—02
20140—01
20150—02
20160—05
20170—03
20180—02
20190—05
20200—04
20210—03
20220—00
20230—08
20240—00
20250—03
20260—0—
Cite this page

510(k) Report. “K002109: Oleeva Foam.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K002109

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