510(k) · Cleared
ClearedKogent Spetzler Lighted Suction Tubes
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Katalyst Surgical, LLC · HBI Illuminator, Fiberoptic, Surgical Field
Cleared on Apr 9, 2015 as substantially equivalent to K113697 (Invuity, Inc., 2012) after a 281-day review. Its family tree reaches back 1 generation to 2012.
- Decided
- Apr 9, 2015
- Review
- 281 days
- Class
- Class II
- Product code
- HBI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K113697 (2012). No later device cites it as a predicate yet.
- Root · 1 generation backK113697 Eigr Surgical Illumination SystemInvuity, Inc. · 2012
- This deviceK141781 Kogent Spetzler Lighted Suction TubesKatalyst Surgical, LLC · 2015
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K113697 | Eigr Surgical Illumination System | Invuity, Inc. | 2012 | — |
| 0 (this device) | K141781 | Kogent Spetzler Lighted Suction Tubes | Katalyst Surgical, LLC | 2015 | — |
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.
Top candidate predicates for a new HBI device
- #1 K223183 Light-Guide Cablesscore 5.0 · 2 generations · no Class I recall
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K113697 | Eigr Surgical Illumination SystemSummary page 4…evice: The Kogent™ Spetzler Lighted Suction Tube was shown to be substantially equivalent to the previously cleared devices: Invuity® Eigr™ Surgical Illumination System, K113697. Page 2 of 3 Substantial Equ… | 2012 |
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?
- Its one ancestor has no recall.
How does its category compare?
All HBI devicesHBI Illuminator, Fiberoptic, Surgical Field: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · HBI
1in 2023
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
MAUDE reports naming product code HBI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 2 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 1 | — | 0 | 3 |
| 2012 | 0 | — | 0 | 2 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 2 |
| 2015 | 1 | — | 0 | 1 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 3 |
| 2018 | 0 | — | 0 | 3 |
| 2019 | 0 | — | 0 | 5 |
| 2020 | 0 | — | 0 | 6 |
| 2021 | 0 | — | 0 | 4 |
| 2022 | 0 | — | 0 | 2 |
| 2023 | 1 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Kogent™ Spetzler Lighted Suction Tubes are intended to provide surgical site illumination from a high intensity light source.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K141781 · printed Nov 6, 2026
Cite this page
510(k) Report. “K141781: Kogent Spetzler Lighted Suction Tubes.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141781
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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