510(k) · Cleared
ClearedAnchor Laparoscopic Tissue Retrieval System, Model TRS100SB
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Anchor Products Co. · GCJ Laparoscope, General & Plastic Surgery
Cleared on Sep 23, 2009 after an 85-day review. The FDA summary names no predicate by number. 11 later devices descend from it.
- Decided
- Sep 23, 2009
- Review
- 85 days
- Class
- Class II
- Product code
- GCJ
- Recalls
- None
- Predicates
- 0
11 later devices descend from it, 3 citing it directly.
- This deviceK091930 Anchor Laparoscopic Tissue Retrieval System, Model TRS100SBAnchor Products Co. · 2009
- Descendant · cites it directly · 6 of its ownK132375 Genistrong Single-Use Specimen Retrieval BagGenicon · 2014 · Recalled
- Descendant · 2 generations on · 2 of its ownK180836 GenistrongGenicon, Inc. · 2018
- Descendant · cites it directly · 2 of its ownK172940 ANCHOR Tissue Retrieval SystemConmed Corporation · 2017 · Recalled
- Descendant · 3 generations on · 1 of its ownK232519 ENDOCOLLECT Specimen Retrieval BagXimedica · 2024
- Descendant · 2 generations on · 1 of its ownK162059 Ezee RetrievalGenicon, Inc. · 2016 · Recalled
Showing 5 of 11 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 11 · See all- K132375Genistrong Single-Use Specimen Retrieval BagGenicon · 2014 · cites it directly6descendants
- K180836GenistrongGenicon, Inc. · 2018 · 2 generations on2descendants
- K172940ANCHOR Tissue Retrieval SystemConmed Corporation · 2017 · cites it directly2descendants
- K232519ENDOCOLLECT Specimen Retrieval BagXimedica · 2024 · 3 generations on1descendant
- K162059Ezee RetrievalGenicon, Inc. · 2016 · 2 generations on1descendant
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K091930 | Anchor Laparoscopic Tissue Retrieval System, Model TRS100SB | Anchor Products Co. | 2009 | — |
| +1 | K132375 | Genistrong Single-Use Specimen Retrieval Bag | Genicon | 2014 | 1 |
| +2 | K180836 | Genistrong | Genicon, Inc. | 2018 | — |
| +1 | K172940 | ANCHOR Tissue Retrieval System | Conmed Corporation | 2017 | 6 |
| +3 | K232519 | ENDOCOLLECT Specimen Retrieval Bag | Ximedica | 2024 | — |
| +2 | K162059 | Ezee Retrieval | Genicon, Inc. | 2016 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 3 | 0 |
| 2019 | 1 | 0 |
| 2024 | 2 | 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?
The FDA summary names no predicate by number.
What descends from it? (11)
See all 113 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?
- Of its descendants, K132375 (Genicon, 2014) has gone furthest, with 6 descendants of its own.
How does its category compare?
All GCJ devicesGCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, 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 Anchor Tissue retrieval system is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during laparoscopic surgery.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K091930 · printed Nov 4, 2026
Cite this page
510(k) Report. “K091930: Anchor Laparoscopic Tissue Retrieval System, Model TRS100SB.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K091930
Report an extraction error
Are you the manufacturer?
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