510(k) Report

510(k) · Cleared

Cleared

troCarWash™ System

K233442510(k) TraditionalCleared May 21, 2024216-day reviewClass II21 CFR 876.1500

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

Biotex, Inc. · OCX Endoscopic Irrigation/Suction System

Cleared on May 21, 2024 as substantially equivalent to K222695 (Biotex, Inc., 2023) after a 216-day review. Its family tree reaches back 6 generations to 1991.

Decided
May 21, 2024
Review
216 days
Class
Class II
Product code
OCX
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K904871 (1991). 25 ancestors in all, the oldest K902683 (1990). No later device cites it as a predicate yet.

  1. Root · 6 generations backK904871 Medi-KleerNorth American Marketing Corp. · 1991
  2. 5 generations backK974454 Clearfield Anti-Fog Sterile Wipe, Product Number 300-004Tucson Medical Corp. · 1997
  3. 4 generations backK062779 Defogging Heated Endoscope Lens Protector (Dhelp); Defogging…New Wave Surgical Corporation · 2006 · Recalled
  4. 3 generations backK080613 Clear-VU System, Models: CVL-01-1000, CVL-01-1030, CVL-01-1045Minimally Invasive Devices, LLC · 2008
  5. 2 generations backK171637 OpClear SystemCipher Surgical, Ltd. · 2018
  6. 1 generation backK222695 troCarWash™ SystemBiotex, Inc. · 2023
  7. This deviceK233442 troCarWash™ SystemBiotex, Inc. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K904871Medi-KleerNorth American Marketing Corp.1991—
−5K974454Clearfield Anti-Fog Sterile Wipe, Product Number 300-004Tucson Medical Corp.1997—
−4K062779Defogging Heated Endoscope Lens Protector (Dhelp); Defogging Endoscope Lens…New Wave Surgical Corporation20062
−3K080613Clear-VU System, Models: CVL-01-1000, CVL-01-1030, CVL-01-1045Minimally Invasive Devices, LLC2008—
−2K171637OpClear SystemCipher Surgical, Ltd.2018—
−1K222695troCarWash™ SystemBiotex, Inc.2023—
0 (this device)K233442troCarWash™ SystemBiotex, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199310
199420
199610
199820
199920
200010
200210
200310
200410
200510
200630
201210
201910
FIG. 1 — Lineage of K233442, 1991–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 OCX? 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 OCX device

  1. #1 K251986 Auxiliary Water Tube Maj-855score 12.8 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K222695troCarWash™ System
Summary page 4
…OCX Legally Marketed Predicate Devices Predicate # Predicate Trade Name (Primary Predicate is listed Product Code first) K222695 troCarWash™ System OCX K102452(Reference) Defogging and cleaning solution – Flo-X…
Biotex, Inc.2023—
†K102452Defogging and Cleaning Solution- Flo-XMinimally Invasive Devices, LLC2010—

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 33 years and passes through 6 companies; a new generation was cleared every 6.3 years on median.
  • 7 of the 25 ancestors have a recall of any class.

How does its category compare?

All OCX devices

OCX Endoscopic Irrigation/Suction System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · OCX

4in 2025

2009: 12010: 32011: 12012: 42013: 32014: 62015: 22016: 22018: 52019: 82020: 42021: 32022: 62023: 72024: 42025: 4
2007high 8 (2019) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OCX

178in 2025

2010: 51 days median2012: 256 days median2013: 106 days median2014: 77 days median2018: 60 days median2019: 133 days median2020: 88 days median2021: 233 days median2022: 84 days median2023: 109 days median2024: 74 days median2025: 178 days median
2007high 256 (2012) · low 51 (2010)2026

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

Recalls per year · OCX

2in 2022

2015: 12020: 112022: 22026 (partial year): 2
2007high 11 (2020) · low 0 (2007)2026

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

Adverse event reports per year · OCX

33in 2025

2008: 12012: 12013: 12014: 52015: 92016: 82017: 92018: 182019: 412020: 112021: 82022: 182023: 462024: 212025: 33
2007high 46 (2023) · low 0 (2007)2025

MAUDE reports naming product code OCX, 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—01
20091—00
201035100
20111—00
2012425601
2013310601
201467705
20152—19
20162—08
20170—09
2018560018
20198133041
20204881111
2021323308
2022684218
20237109046
2024474021
20254178033
20260—2—

What is it indicated for?

The troCarWash™ system consists of a reusable control unit and a disposable, sterile, single-use trocar intended to remove visual obstructions such as condensation, blood, and other tissue particulates from the distal lens of a laparoscope during surgery and therefore maintain a clear image of the surgical site.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K233442: troCarWash™ System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K233442

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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