510(k) Report

510(k) · Cleared

Cleared

Microline Inc. Reusable Laparoscopic Clip Applier with Implantable Titanium Clips, Model M/L-10

K013695510(k) TraditionalCleared Jan 8, 200262-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

Microline Pentax, Inc. · GCJ Laparoscope, General & Plastic Surgery

Cleared on Jan 8, 2002 after a 62-day review. The FDA summary names its predicate without a number. 3 later devices descend from it.

Decided
Jan 8, 2002
Review
62 days
Class
Class II
Product code
GCJ
Recalls
None
Predicates
0

3 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2015: 1 descendant cleared2025: 2 descendants cleared200020052010201520202025
  1. This deviceK013695 Microline Inc. Reusable Laparoscopic Clip Applier with Implantable…Microline Pentax, Inc. · 2002
  2. Descendant · cites it directly · 2 of its ownK150259 CLIP PLUS Disposable Clip Applier,ML;CLIP PLUS Disposable Clip…Taiwan Surgical Corporation · 2015
  3. Descendant · 2 generations on · 0 of its ownK253781 InnoClip Clip ApplierTaiwan Surgical Corporation · 2025
  4. Descendant · 2 generations on · 0 of its ownK253903 InnoClip Disposable Clip ApplierTaiwan Surgical Corporation · 2025

Most influential descendants

Showing 3 of 3 · See all
  • K150259CLIP PLUS Disposable Clip Applier,ML;CLIP PLUS Disposable Clip Applier,LTaiwan Surgical Corporation · 2015 · cites it directly2descendants
  • K253781InnoClip Clip ApplierTaiwan Surgical Corporation · 2025 · 2 generations on0descendants
  • K253903InnoClip Disposable Clip ApplierTaiwan Surgical Corporation · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K013695Microline Inc. Reusable Laparoscopic Clip Applier with Implantable Titanium…Microline Pentax, Inc.2002—
+1K150259CLIP PLUS Disposable Clip Applier,ML;CLIP PLUS Disposable Clip Applier,LTaiwan Surgical Corporation2015—
+2K253781InnoClip Clip ApplierTaiwan Surgical Corporation2025—
+2K253903InnoClip Disposable Clip ApplierTaiwan Surgical Corporation2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
202520
FIG. 1 — Lineage of K013695, 2002–2025Source: 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? (2)

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
*—Applied Medical
Named without a submission number
—
*—Ethicon Endosurgery
Named without a submission number
—

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K150259CLIP PLUS Disposable Clip Applier,ML;CLIP PLUS Disposable Clip Applier,LTaiwan Surgical Corporation20152

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, K150259 (Taiwan Surgical Corporation, 2015) has gone furthest, with 2 descendants of its own.

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.

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?

To occlude and ligate vessels, ducts, tracts, and other tubular structures during Laparoscopic and general surgical procedures

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. “K013695: Microline Inc. Reusable Laparoscopic Clip Applier with Implantable Titanium Clips, Model M/L-10.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K013695

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026