510(k) Report

510(k) · Cleared

Cleared

U-IGNITE Bladeless Trocar

K162387510(k) TraditionalCleared Jan 11, 2017139-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

Tianjin Uwell Medical Device Manufacturing Co., Ltd. · GCJ Laparoscope, General & Plastic Surgery

Cleared on Jan 11, 2017 as substantially equivalent to K122511 (Ethicon Endo-Surgery, LLC, 2012) after a 139-day review. Its family tree reaches back 2 generations to 2003. 1 later device descends from it.

Decided
Jan 11, 2017
Review
139 days
Class
Class II
Product code
GCJ
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K032676 (2003). 1 later device descends from it, 1 citing it directly.

  1. Root · 2 generations backK032676 Endopath Bladeless Trocar, Endopath Blunt Tip Trocar, Endopath…Ethicon Endo-Surgery, Inc. · 2003 · Recalled
  2. 1 generation backK122511 Endopath Xcel Bladeless Trocar with Optiview Technology Endopath…Ethicon Endo-Surgery, LLC · 2012
  3. This deviceK162387 U-IGNITE Bladeless TrocarTianjin Uwell Medical Device Manufacturing Co., Ltd. · 2017
  4. Descendant · cites it directly · 0 of its ownK202931 Disposable TrocarWuxi Shukang Medical Appliance Co., Ltd. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K202931Disposable TrocarWuxi Shukang Medical Appliance Co., Ltd. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K032676Endopath Bladeless Trocar, Endopath Blunt Tip Trocar, Endopath Dilating Tip…Ethicon Endo-Surgery, Inc.20036
−1K122511Endopath Xcel Bladeless Trocar with Optiview Technology Endopath Xcel Blunt…Ethicon Endo-Surgery, LLC2012—
0 (this device)K162387U-IGNITE Bladeless TrocarTianjin Uwell Medical Device Manufacturing Co., Ltd.2017—
+1K202931Disposable TrocarWuxi Shukang Medical Appliance Co., Ltd.2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K162387, 2003–2020Source: 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 GCJ? 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 GCJ device

  1. #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 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? (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
*K122511Endopath Xcel Bladeless Trocar with Optiview Technology Endopath Xcel Blunt Tip Trocar…
Summary page 4
…Product 510(k) Code Number ENDOPATH XCEL Ethicon Endo-Surgery, GCJ K122511 Bladeless Trocar with LLC OPTI VIEW Technology Reference Device: Device Company Product…
Ethicon Endo-Surgery, LLC2012—
†K141594Unimicro Trocar Kit, models: Auto-Locking Trocar, Hasson Trocar, Bladeless TrocarUnimicro Medical Systems (Shenzhen) Co., Ltd.2015—

Also cleared against K122511: 6 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K202931Disposable TrocarWuxi Shukang Medical Appliance Co., Ltd.20200

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 14 years and passes through 3 companies; a new generation was cleared every 8.9 years on median.
  • 1 of the 2 ancestors has a recall of any class.
  • Of its descendants, K202931 (Wuxi Shukang Medical Appliance Co., Ltd., 2020) has gone furthest, with 0 descendants of its own.
  • 6 other devices also cite its predicate K122511.

How does its category compare?

All GCJ devices

GCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · GCJ

21in 2025

2007: 182008: 192009: 212010: 242011: 152012: 172013: 152014: 192015: 262016: 272017: 202018: 212019: 152020: 282021: 182022: 202023: 312024: 292025: 212026 (partial year): 26
2007high 31 (2023) · low 15 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GCJ

108in 2025

2007: 42 days median2008: 73 days median2009: 85 days median2010: 122 days median2011: 113 days median2012: 88 days median2013: 93 days median2014: 90 days median2015: 76 days median2016: 99 days median2017: 77 days median2018: 88 days median2019: 60 days median2020: 61 days median2021: 116 days median2022: 103 days median2023: 109 days median2024: 90 days median2025: 108 days median2026 (partial year): 122 days median
2007high 122 (2010) · low 42 (2007)2026

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

Recalls per year · GCJ

5in 2025

2007: 122008: 162009: 62010: 302011: 92012: 12013: 7, 1 Class I2014: 22016: 52017: 12018: 12022: 12023: 12025: 52026 (partial year): 1
2007high 30 (2010) · low 0 (2015)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GCJ

5,860in 2025

2007: 1,6392008: 1,3192009: 1,9952010: 2,6572011: 2,1332012: 1,5262013: 1,5652014: 1,7142015: 1,7102016: 2,0802017: 3,4682018: 2,5622019: 2,5782020: 2,6182021: 3,4312022: 3,9452023: 6,0022024: 6,0472025: 5,860
2007high 6,047 (2024) · low 1,319 (2008)2025

MAUDE reports naming product code GCJ, 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
20071842121,639
20081973161,319
2009218561,995
201024122302,657
20111511392,133
2012178811,526
201315937 (1)1,565
2014199021,714
2015267601,710
2016279952,080
2017207713,468
2018218812,562
2019156002,578
2020286102,618
20211811603,431
20222010313,945
20233110916,002
2024299006,047
20252110855,860
2026261221—

What is it indicated for?

The U-IGNITE Bladeless Trocar has applications in endoscopic procedures to provide a port of entry for endoscopic instruments.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K162387: U-IGNITE Bladeless Trocar.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K162387

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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