510(k) Report

510(k) · Cleared

Cleared

Light-Guide Cables

K223183510(k) TraditionalCleared Jan 13, 202393-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

Olympus Winter & Ibe GmbH · HBI Illuminator, Fiberoptic, Surgical Field

Cleared on Jan 13, 2023 as substantially equivalent to K111342 (Schott North America, 2011) after a 93-day review. Its family tree reaches back 2 generations to 1999.

Decided
Jan 13, 2023
Review
93 days
Class
Class II
Product code
HBI
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K991208 (1999). No later device cites it as a predicate yet.

  1. Root · 2 generations backK991208 Endoscopic Fiberoptic CableIsolux America · 1999
  2. 1 generation backK111342 Light Guide CableSchott North America · 2011
  3. This deviceK223183 Light-Guide CablesOlympus Winter & Ibe GmbH · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K991208Endoscopic Fiberoptic CableIsolux America1999—
−1K111342Light Guide CableSchott North America2011—
0 (this device)K223183Light-Guide CablesOlympus Winter & Ibe GmbH2023—
FIG. 1 — Lineage of K223183, 1999–2023Source: 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 HBI? 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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What was it cleared against? (1)

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
*K111342Light Guide Cable
Summary page 4
…ct code / No. Reg No. Light Guide Cable HBI / 21 CFR K111342 not stated in K111342 Schott North America 878.4…
Schott North America2011—

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 24 years and passes through 3 companies; a new generation was cleared every 12.4 years on median.
  • None of the 2 ancestors has a recall.

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. 2023, this device’s year, is highlighted.

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—

What is it indicated for?

Transmission of light energy from the light source to an optical instrument.

The light-guide cable is used to transmit light during endoscopic procedures or for other medical illumination application when the properties and operating instructions are complied with.

The light-guide cable is designed for use with halogen, xenon or LED based light sources of cold light which are utilized in medical applications that involve endoscopes, medical instruments or microscopes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223183: Light-Guide Cables.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K223183

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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