510(k) Report

510(k) · Cleared

Cleared

Sterilucent Self-Contained Biological Indicator

K141238510(k) TraditionalCleared Nov 3, 2014174-day reviewClass II21 CFR 880.2800

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

Sterilucent, Inc. · FRC Indicator, Biological Sterilization Process

Cleared on Nov 3, 2014 as substantially equivalent to K102884 (Advanced Sterilization Products, 2011) and 1 other predicate after a 174-day review. Its family tree reaches back 4 generations to 2002.

Decided
Nov 3, 2014
Review
174 days
Class
Class II
Product code
FRC
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K994055 (2002). 5 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 4 generations backK994055 Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2002 · Recalled
  2. 3 generations backK031226 Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2003 · Recalled
  3. 2 generations backK071014 Modification to Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products · 2007
  4. 1 generation backK102884 Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products · 2011
  5. This deviceK141238 Sterilucent Self-Contained Biological IndicatorSterilucent, Inc. · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K994055Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products20021
−3K031226Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products20031
−2K071014Modification to Sterrad Cyclesure Biological IndicatorAdvanced Sterilization Products2007—
−1K102884Sterrad Cyclesure 24 Biological IndicatorAdvanced Sterilization Products2011—
0 (this device)K141238Sterilucent Self-Contained Biological IndicatorSterilucent, Inc.2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201310
FIG. 1 — Lineage of K141238, 2002–2014Source: 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), 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 FRC? 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 FRC device

  1. #1 K250044 Celerity 5 HP Biological Indicator (LCB052)…score 14.5 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K102884Sterrad Cyclesure 24 Biological Indicator
Summary page 5
…Device Class: Class II Product Code: FRC (21 CFR 880.2800) 2. Predicate Device STERRAD® CycleSure® 24 Biological Indicator (K102884) Smart-Well Model 1710 EZTest Incubator (K122362) 3. Device Description The Sterilucent Self-Contained Biological Indica…
Advanced Sterilization Products2011—
*K122362Smart-Well Incubator
Summary page 5
…uct Code: FRC (21 CFR 880.2800) 2. Predicate Device STERRAD® CycleSure® 24 Biological Indicator (K102884) Smart-Well Model 1710 EZTest Incubator (K122362) 3. Device Description The Sterilucent Self-Contained Biological Indicator is a self-contained biological indicator (SCB…
Mesa Laboratories, Inc.2013—

Also cleared against K102884: 1 other device →

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.

What does this lineage say?

  • The line of descent spans 12 years and passes through 2 companies; a new generation was cleared every 3.8 years on median.
  • 2 of the 5 ancestors have a recall of any class.
  • 1 other device also cites its predicate K102884.

How does its category compare?

All FRC devices

FRC Indicator, Biological Sterilization Process: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · FRC

6in 2025

2007: 32008: 12009: 62010: 42011: 62012: 92013: 42014: 132015: 32016: 22017: 102018: 182019: 52020: 102021: 52022: 52023: 62024: 82025: 62026 (partial year): 1
2007high 18 (2018) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRC

29in 2025

2007: 83 days median2009: 183 days median2010: 165 days median2011: 118 days median2012: 178 days median2013: 260 days median2014: 174 days median2015: 130 days median2017: 130 days median2018: 97 days median2019: 88 days median2020: 150 days median2021: 107 days median2022: 193 days median2023: 190 days median2024: 105 days median2025: 29 days median
2007high 260 (2013) · low 29 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FRC

8so far in 2026, the most since 2007

2009: 12012: 22013: 22022: 42023: 12026 (partial year): 8
2007high 8 (2026) · low 0 (2007)2026

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

Adverse event reports per year · FRC

9in 2025

2007: 1002008: 602009: 452010: 572011: 372012: 462013: 392014: 512015: 1822016: 4822017: 1822018: 222019: 302020: 162021: 102022: 92023: 202024: 222025: 9
2007high 482 (2016) · low 9 (2022)2025

MAUDE reports naming product code FRC, 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
20073830100
20081—060
20096183145
20104165057
20116118037
20129178246
20134260239
201413174051
201531300182
20162—0482
2017101300182
20181897022
2019588030
202010150016
20215107010
2022519349
20236190120
20248105022
202562909
20261—8—

What is it indicated for?

The Sterilucent Self-Contained Biological Indicator is for monitoring the efficacy of the hydrogen peroxide sterilization process in the Sterilucent PSD-85 Sterilizer Lumen and Non-Lumen cycles. It is intended for use solely in a test pack.

The Sterilucent Biological Indicator Monitoring System is intended for incubating and monitoring of the Sterilucent Self-Contained Biological Indicator.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141238: Sterilucent Self-Contained Biological Indicator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141238

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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