510(k) · Cleared
ClearedAsc Triport Laparoscopic Access Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Advanced Surgical Concepts · GCJ Laparoscope, General & Plastic Surgery
Cleared on Jan 29, 2008 as substantially equivalent to K073170 (Advanced Surgical Concepts, 2007) and 4 other predicates after a 29-day review. Its family tree reaches back 3 generations to 2001. 13 later devices descend from it.
- Decided
- Jan 29, 2008
- Review
- 29 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 5
Its longest line of descent runs back 3 generations to K010007 (2001). 6 ancestors in all. 13 later devices descend from it, 5 citing it directly.
- Root · 3 generations backK010007 Adapt Laparoscopic Port & Adapt Reducer CapTaut, Inc. · 2001 · Recalled
- 2 generations backK070158 R-Port Laparoscopic Access DeviceAdvanced Surgical Concepts · 2007
- 1 generation backK073170 R-Port II Laparoscopic Access DeviceAdvanced Surgical Concepts · 2007
- This deviceK073719 Asc Triport Laparoscopic Access DeviceAdvanced Surgical Concepts · 2008
- Descendant · cites it directly · 5 of its ownK100045 OCTODalim Surgnet Corporation · 2010
- Descendant · 2 generations on · 4 of its ownK112196 OctotmportDalim Surgnet Corporation · 2011
- Descendant · cites it directly · 4 of its ownK101794 Asc Triport Laparoscopic Access Device Model TPRT-02-01 (WA58000T)…Advanced Surgical Concepts · 2010
- Descendant · cites it directly · 3 of its ownK141715 Glove PortNelis · 2015
- Descendant · 2 generations on · 3 of its ownK110004 Asc Triport+ Laparoscopic Access DeviceAdvanced Surgical Concepts · 2011
Showing 5 of 13 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 13 · See all- K100045OCTODalim Surgnet Corporation · 2010 · cites it directly5descendants
- K112196OctotmportDalim Surgnet Corporation · 2011 · 2 generations on4descendants
- K101794Asc Triport Laparoscopic Access Device Model TPRT-02-01 (WA58000T), Asc Quadport…Advanced Surgical Concepts · 2010 · cites it directly4descendants
- K141715Glove PortNelis · 2015 · cites it directly3descendants
- K110004Asc Triport+ Laparoscopic Access DeviceAdvanced Surgical Concepts · 2011 · 2 generations on3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K010007 | Adapt Laparoscopic Port & Adapt Reducer Cap | Taut, Inc. | 2001 | 3 |
| −2 | K070158 | R-Port Laparoscopic Access Device | Advanced Surgical Concepts | 2007 | — |
| −1 | K073170 | R-Port II Laparoscopic Access Device | Advanced Surgical Concepts | 2007 | — |
| 0 (this device) | K073719 | Asc Triport Laparoscopic Access Device | Advanced Surgical Concepts | 2008 | — |
| +1 | K100045 | OCTO | Dalim Surgnet Corporation | 2010 | — |
| +2 | K112196 | Octotmport | Dalim Surgnet Corporation | 2011 | — |
| +1 | K101794 | Asc Triport Laparoscopic Access Device Model TPRT-02-01 (WA58000T), Asc… | Advanced Surgical Concepts | 2010 | — |
| +1 | K141715 | Glove Port | Nelis | 2015 | — |
| +2 | K110004 | Asc Triport+ Laparoscopic Access Device | Advanced Surgical Concepts | 2011 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
| 2003 | 1 | 0 |
| 2006 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2010 | 3 | 0 |
| 2011 | 2 | 0 |
| 2012 | 3 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 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? (5)
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 |
|---|---|---|---|
| * | K073170 | R-Port II Laparoscopic Access DeviceSummary page 1…Accessory Classification Name: Endoscopic Accessory and Surgical Retractor 3. PREDICATE DEVICES * R-Port II Laparoscopic Access Device subject of K073170 * R-Port Laparoscopic Access Device subject of K070158 * Taut Inc. ADAPt Laparoscopic Port and Accessory subject of… | 2007 |
| * | K070158 | R-Port Laparoscopic Access DeviceSummary page 1…ry and Surgical Retractor 3. PREDICATE DEVICES * R-Port II Laparoscopic Access Device subject of K073170 * R-Port Laparoscopic Access Device subject of K070158 * Taut Inc. ADAPt Laparoscopic Port and Accessory subject of KO10007 • Ethicon Endopath III Trocar System subject o… | 2007 |
| * | K010007 | Adapt Laparoscopic Port & Adapt Reducer Cap | 2001 |
| * | K032676 | Endopath Bladeless Trocar, Endopath Blunt Tip Trocar, Endopath Dilating Tip TrocarSummary page 1…copic Access Device subject of K070158 * Taut Inc. ADAPt Laparoscopic Port and Accessory subject of KO10007 • Ethicon Endopath III Trocar System subject of K032676 • ASC Ecotract Device subject of K01071 I 4. DEVICE DESCRIPTION The ASC TriPort Laparoscopic Access Device is a l… | 2003 |
| * | K010711 | Ecotract Adjustable Wound Protector/Retractor | 2001 |
What descends from it? (13)
See all 135 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)
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 7 years and passes through 2 companies; a new generation was cleared every 3 months on median.
- 2 of the 6 ancestors have a recall of any class.
- Of its descendants, K100045 (Dalim Surgnet Corporation, 2010) has gone furthest, with 5 descendants of its own.
- 2 other devices also cite its predicate K073170.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, 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 ASC TriPort Laparoscopic Access Device is intended for use as a multiple instrument and/or camera port during minimally invasive abdominal laparoscopic surgery.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K073719 · printed Nov 4, 2026
Cite this page
510(k) Report. “K073719: Asc Triport Laparoscopic Access Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K073719
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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