510(k) Report

510(k) · Cleared

Cleared

1125 XSB Xenon Fiber-Optic Light Source

K052979510(k) TraditionalCleared Oct 31, 20057-day reviewClass II21 CFR 878.4580

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

Isolux, LLC · HBI Illuminator, Fiberoptic, Surgical Field

Cleared on Oct 31, 2005 after a 7-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Oct 31, 2005
Review
7 days
Class
Class II
Product code
HBI
Recalls
None
Predicates
0

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

Descendants, by year cleared 2007: 1 descendant cleared20052010201520202025
  1. This deviceK052979 1125 XSB Xenon Fiber-Optic Light SourceIsolux, LLC · 2005
  2. Descendant · cites it directly · 0 of its ownK070287 PS Series with Fiber Light Guide and Headlight, Models PS200, PS250…Photonic Optische Gerate GmbH & Cokg · 2007

Most influential descendants

Showing 1 of 1 · See all
  • K070287PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500Photonic Optische Gerate GmbH & Cokg · 2007 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K0529791125 XSB Xenon Fiber-Optic Light SourceIsolux, LLC2005—
+1K070287PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500Photonic Optische Gerate GmbH & Cokg2007—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K052979, 2005–2007Source: 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.

Planning a device in HBI? 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 HBI device

  1. #1 K223183 Light-Guide Cablesscore 5.0 · 2 generations · no Class I recall
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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? (1)

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

NumberDeviceApplicantDecidedDescendants
K070287PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500Photonic Optische Gerate GmbH & Cokg20070

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, K070287 (Photonic Optische Gerate GmbH & Cokg, 2007) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HBI devices

HBI Illuminator, Fiberoptic, Surgical Field: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · HBI

1in 2023

2011: 12015: 12016: 12023: 1
2007high 1 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HBI

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

Recalls per year · HBI

No recall names HBI since 2007.

Adverse event reports per year · HBI

1in 2025

2008: 22009: 12011: 32012: 22013: 12014: 22015: 12017: 32018: 32019: 52020: 62021: 42022: 22023: 12024: 22025: 1
2007high 6 (2020) · low 0 (2007)2025

MAUDE reports naming product code HBI, 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—02
20090—01
20100—00
20111—03
20120—02
20130—01
20140—02
20151—01
20161—00
20170—03
20180—03
20190—05
20200—06
20210—04
20220—02
20231—01
20240—02
20250—01
20260—0—
Cite this page

510(k) Report. “K052979: 1125 XSB Xenon Fiber-Optic Light Source.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K052979

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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