510(k) · Cleared
Recalled · Class II · 2017Kii Trocar System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Applied Medical Resources Corp. · GCJ Laparoscope, General & Plastic Surgery
Cleared on Oct 5, 2007 as substantially equivalent to K060096 (Applied Medical Resources Corp., 2006) and 2 other predicates after a 14-day review. Its family tree reaches back 3 generations to 1999. 2 later devices descend from it. It has been recalled 2 times.
- Decided
- Oct 5, 2007
- Review
- 14 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- 2
- Predicates
- 3
Its longest line of descent runs back 3 generations to K990028 (1999). 7 ancestors in all, the oldest K932995 (1993). 2 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK990028 Endopath Optiview Optical Surgical Obturator and SleeveEthicon Endo-Surgery, Inc. · 1999
- 2 generations backK032889 Optical SeparatorApplied Medical Resources · 2003
- 1 generation backK060096 Modular Trocar SystemApplied Medical Resources Corp. · 2006 · Recalled
- This deviceK072674 Kii Trocar SystemApplied Medical Resources Corp. · 2007
- Descendant · cites it directly · 0 of its ownK231400 Bladeless Trocar – Artemis Lap CannulaT.A.G. Medical Products Corporation, Ltd. · 2023
- Descendant · cites it directly · 0 of its ownK111002 Reprocessed Endoscopic TrocarsSterilmed, Inc. · 2011
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K990028 | Endopath Optiview Optical Surgical Obturator and Sleeve | Ethicon Endo-Surgery, Inc. | 1999 | — |
| −2 | K032889 | Optical Separator | Applied Medical Resources | 2003 | — |
| −1 | K060096 | Modular Trocar System | Applied Medical Resources Corp. | 2006 | 7 |
| 0 (this device) | K072674 | Kii Trocar System | Applied Medical Resources Corp. | 2007 | — |
| +1 | K231400 | Bladeless Trocar – Artemis Lap Cannula | T.A.G. Medical Products Corporation, Ltd. | 2023 | — |
| +1 | K111002 | Reprocessed Endoscopic Trocars | Sterilmed, Inc. | 2011 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1993 | 1 | 0 |
| 1994 | 1 | 0 |
| 1997 | 1 | 0 |
| 2002 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2023 | 1 | 0 |
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 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K060096 | Modular Trocar SystemSummary page 1…876.1500) TRADE NAME: Kii Shielded Access System PREDICATE DEVICE: Applied Medical Modular Trocar System (K060096) Applied Medical Disposable Surgical Trocar (K943489) Ethicon… | 2006 |
| * | K943489 | Disposable Surgical TrocarSummary page 1…s System PREDICATE DEVICE: Applied Medical Modular Trocar System (K060096) Applied Medical Disposable Surgical Trocar (K943489) Ethicon Bladed Shielded System (K971475) INTENDED USE: The Modular Trocar System is a sterile… | 1994 |
| * | K971475 | Shielded Surgical TrocarSummary page 1…System (K060096) Applied Medical Disposable Surgical Trocar (K943489) Ethicon Bladed Shielded System (K971475) INTENDED USE: The Modular Trocar System is a sterile, single-use device, intended for use in conjunction with APPLIED's current… | 1997 |
What descends from it? (2)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| May 4, 2017 | Class II | Z-2533-2017 | Under Investigation by firm | Due to possibility of insufficient sterilization. |
| Nov 5, 2012 | Class II | Z-0644-2013 | Nonconforming Material/Component | Applied Medical is conducting a voluntary recall on a specific lot number of its 12x150mm Kii shielded bladed access systems. This is due to a potential for the blade to remain exposed after shield deployment. Further use of any affected… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 8 years and passes through 3 companies; a new generation was cleared every 2.3 years on median.
- 2 of the 7 ancestors have a recall of any class.
- Of its descendants, K231400 (T.A.G. Medical Products Corporation, Ltd., 2023) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K060096.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · GCJ
21in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GCJ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GCJ
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GCJ
5,860in 2025
MAUDE reports naming product code GCJ, 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 | 18 | 42 | 12 | 1,639 |
| 2008 | 19 | 73 | 16 | 1,319 |
| 2009 | 21 | 85 | 6 | 1,995 |
| 2010 | 24 | 122 | 30 | 2,657 |
| 2011 | 15 | 113 | 9 | 2,133 |
| 2012 | 17 | 88 | 1 | 1,526 |
| 2013 | 15 | 93 | 7 (1) | 1,565 |
| 2014 | 19 | 90 | 2 | 1,714 |
| 2015 | 26 | 76 | 0 | 1,710 |
| 2016 | 27 | 99 | 5 | 2,080 |
| 2017 | 20 | 77 | 1 | 3,468 |
| 2018 | 21 | 88 | 1 | 2,562 |
| 2019 | 15 | 60 | 0 | 2,578 |
| 2020 | 28 | 61 | 0 | 2,618 |
| 2021 | 18 | 116 | 0 | 3,431 |
| 2022 | 20 | 103 | 1 | 3,945 |
| 2023 | 31 | 109 | 1 | 6,002 |
| 2024 | 29 | 90 | 0 | 6,047 |
| 2025 | 21 | 108 | 5 | 5,860 |
| 2026 | 26 | 122 | 1 | — |
What is it indicated for?
The Applied Medical Modular Trocar System is a sterile, single-use device consisting of a bladed, shielded obturator, a cannula and seal. The obturator and seal may also be used with reusable APPLIED cannulas that may be made of stainless steel or DuraGold® polymer. The obturator is intended for use in conjunction with APPLIED'S currently marketed trocar products to establish a path of entry for endoscopic instruments for use during general, abdominal, gynecological and thoracic minimally invasive procedures or to gain access through tissue planes and/or potential spaces for endoscopic instruments.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K072674 · printed Nov 4, 2026
Cite this page
510(k) Report. “K072674: Kii Trocar System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K072674
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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